Selective androgen receptor degrader (sard) ligands and methods of use thereof

ABSTRACT

This invention is directed to pyrrole, pyrazole, imidazole, triazole, and morpholine based selective androgen receptor degrader (SARD) compounds including cyclic and heterocyclic anilide rings and their synthetic precursors, and mono-, di-, or multi-substituted N-heterocyclic rings, R-isomers, non-hydroxylated and/or non-chiral propanamides in treating androgen receptor dependent diseases and conditions such as hyperproliferations of the prostate including pre-malignancies and benign prostatic hyperplasia, prostate cancer, advanced prostate cancer, castration resistant prostate cancer, triple negative breast cancer, other cancers expressing the androgen receptor, androgenic alopecia or other hyperandrogenic dermal diseases, Kennedy&#39;s disease, amyotrophic lateral sclerosis (ALS), abdominal aortic aneurysm (AAA), and uterine fibroids, and to methods for reducing the levels of androgen receptor-full length (AR-FL) including pathogenic or resistance mutations, AR-splice variants (AR-SV), and pathogenic polyglutamine (polyQ) polymorphisms of AR in a subject.

FIELD OF THE INVENTION

This invention is directed to pyrrole, pyrazole, imidazole, triazole,and morpholine based selective androgen receptor degrader (SARD)compounds including cyclic and heterocyclic anilide rings and theirsynthetic precursors and mono-, di-, or multi-substituted N-heterocyclicrings, R-isomers, non-hydroxylated and/or non-chiral propanamides intreating androgen receptor dependent diseases and conditions such ashyperproliferations of the prostate including pre-malignancies andbenign prostatic hyperplasia, prostate cancer, advanced prostate cancer,castration resistant prostate cancer, triple negative breast cancer,other cancers expressing the androgen receptor, androgenic alopecia orother hyperandrogenic dermal diseases. Kennedy's disease, amyotrophiclateral sclerosis (ALS), abdominal aortic aneurysm (AAA), and uterinefibroids, and to methods for reducing the levels of androgenreceptor-full length (AR-FL) including pathogenic or resistancemutations, AR-splice variants (AR-SV), and pathogenic polyglutamine(polyQ) polymorphisms of AR in a subject.

BACKGROUND OF THE INVENTION

Prostate cancer (PCa) is one of the most frequently diagnosednoncutaneous cancers among men in the US and is the second most commoncause of cancer deaths with more than 200,000 new cases and over 30,000deaths each year in the United States. PCa therapeutics market isgrowing at an annual rate of 15-20% globally.

Androgen-deprivation therapy (ADT) is the standard of treatment foradvanced PCa. Patients with advanced prostate cancer undergo ADT, eitherby luteinizing hormone releasing hormone (LHRH) agonists, LHRHantagonists or by bilateral orchiectomy. Despite initial response toADT, disease progression is inevitable and the cancer emerges ascastration-resistant prostate cancer (CRPC). Up to 30% of patients withprostate cancer that undergo primary treatment by radiation or surgerywill develop metastatic disease within 10 years of the primarytreatment. Approximately 50,000 patients a year will develop metastaticdisease, which is termed metastatic CRPC (mCRPC).

Patients with CRPC have a median survival of 12-18 months. Thoughcastration-resistant, CRPC is still dependent on the androgen receptor(AR) signaling axis for continued growth. The primary reason for CRPCre-emergence is re-activation of AR by alternate mechanisms such as: 1)intracrine androgen synthesis, 2) AR splice variants (AR-SV), e.g.. thatlack ligand binding domain (LBD), 3) AR-LBD mutations with potential toresist AR antagonists (i.e., mutants that are not sensitive toinhibition by AR antagonists, and in some cases AR antagonists act asagonists of the AR bearing these LBD mutations), 4) amplifications ofthe AR gene within the tumor (e.g., as driven by the fusion of othergenes such as the ETS family of transcription factors (see for examplePMID: 20478527, 30033370), and 5) rearrangements of the AR gene withinthe tumor, e.g., as described in PMID: 27897170. A critical harrier toprogress in treating CRPC is that AR signaling inhibitors such asenzalutamide, bicalutamide, and abiraterone, acting through the LBD,fail to inhibit growth driven by the N-terminal domain (NTD)-dependentconstitutively active AR-SV such as AR-V7, the most prominent AR-SV.Recent high-impact clinical trials with enzalutamide and abiraterone inCRPC patients demonstrated that just 13.9% of AR-V7positive patientsamong 202 patients starting treatment with enzalutamide (Xtandi) orabiraterone acetate (Zytiga) had PSA responses to either of thetreatments (Antonarakis E S. Lu C. Luber B. et al. J. Clin. Oncol. 2017Apr. 6. doi: 10.1200/X0.2016.70.1961), indicating the requirement fornext generation AR antagonists that target AR-SVs. In addition, asignificant number of CRPC patients are becoming refractory toabiraterone or enzalutamide, emphasizing the need for next generation ARantagonists.

Current evidences demonstrate that CRPC growth is dependent onconstitutively active AR including AR-SV's that lack the LBD such asAR-V7 and therefore cannot be inhibited by conventional antagonists. ARinhibition and degradation through binding to a domain that is distinctfrom the AR LBD provides alternate strategies to manage CRPC.

Herein the NTD is biophysically characterized to interact with the SARDsof this invention via fluorescence polarization (FP) and NMR (Example9). Biochemical evidence also supports the SARDs of this inventionbinding to a domain other than the LBD. E.g., SARDs of this inventiondegrade AR-SV in D567es cells lacking the expression of any ARcontaining the LBD (Example 5). Further, the R- and S-isomers of theSARDs of this invention possess equipotent SARD activity despitedemonstrated differences in the binding and inhibition ofandrogen-dependent transactivation via the LBD (Examples 3 and 4). Thereport of SARD activity mediated through the NTD of AR is anunprecedented observation that may help explanation the prodigious ARantagonism profiles seen with the SARDs of this invention.

Molecules that degrade the AR prevent any inadvertent AR activationthrough growth factors or signaling pathways, or promiscuousligand-dependent activation. In addition, molecules that inhibit theconstitutive activation of AR-SVs are extremely important to provideextended benefit to CRPC patients.

Currently only a few chemotypes are known to degrade AR which includethe SARDs ARN-509, AZD-35 14, and ASC-19. However. these moleculesdegrade AR indirectly at much higher concentrations than their bindingcoefficient and they fail to degrade the AR-SVs that have become inrecent years the primary reason for resurgence of treatment-resistantCRPC.

This invention describes novel AR antagonists with unique pharmacologythat strongly (high potency and efficacy) and selectively hind AR(better than known antagonists in some cases; bind to LBD and/or NTD),antagonize AR, and degrade AR full length (AR-FL) and AR-SV. Selectiveandrogen receptor degrader (SARD) compounds possess dual degradation andAR-SV inhibitory functions and hence are distinct from any availableCRPC therapeutics. These novel selective androgen receptor degrader(SARD) compounds inhibit the growth of PCa cells and tumors that aredependent on AR-FL and AR-SV for proliferation.

SARDs have the potential to evolve as new therapeutics to treat CRPCsthat are untreatable with any other antagonists. This unique property ofdegrading AR-SV has extremely important health consequences for prostatecancer. Till date only one series of synthetic molecules (EPI-001,EPI-506, etc.) and some marine natural products such as the sinkotamidesand glycerol ether Naphetenone B, are reported to hind to AR-NTD andinhibit AR function and PCa cell growth, albeit at lower affinity andinability to degrade the receptor. The SARDs reported herein also bindto AR-NTD and inhibit NTD-driven (e.g., ligand independent) AR activity.

The positive correlation between AR and PCa and the lack of a fail-safeAR antagonist, emphasizes the need for molecules that inhibit ARfunction through novel or alternate mechanisms and/or binding sites, andthat can elicit antagonistic activities within an altered cellularenvironment.

Although traditional antiandrogens such as enzalutamide. bicalutamideand flutamide and androgen deprivation therapies (ADT) were approved foruse in prostate cancer, there is significant evidence that antiandrogenscould also be used in a variety of other hormone dependent and hormoneindependent cancers. For example, antiandrogens have been tested inbreast cancer (enzalutamide; Breast Cancer Res. (2014) 16(1): R7).non-small cell lung cancer (shRNAi AR). renal cell carcinoma (ASC-J9),partial androgen insensitivity syndrome (PAIS) associated malignanciessuch as gonadal tumors and seminoma, advanced pancreatic cancer (WorldJ. Gastroenterology 20(29). 9229), cancer of the ovary, fallopian tubes,or peritoneum, cancer of the salivary gland (Head and Neck (2016) 38.724-731; ADT was tested in AR-expressing recurrent/metastatic salivarygland cancers and was confirmed to have benefit on progression freesurvival and overall survival endpoints), bladder cancer (Oncotarget6(30), 29860-29876); Int J. Endocrinol (2015), Article ID 384860),pancreatic cancer, lymphoma (including mantle cell), and hepatocellularcarcinoma. Use of a more potent antiandrogen such as a SARD in thesecancers may more efficaciously treat the progression of these and othercancers. Other cancers may also benefit from SARD treatment such asbreast cancer (e.g., triple negative breast cancer (TNBC)), testicularcancer, cancers associated with partial androgen insensitivity syndromes(PAIS) such as gonadal tumors and seminoma, uterine cancer, ovariancancer, cancer of the fallopian tubes or peritoneum, salivary glandcancer, bladder cancer, urogenital cancer, brain cancer, skin cancer,lymphoma, mantle cell lymphoma, liver cancer, hepatocellular carcinoma,renal cancer, renal cell carcinoma, osteosarcoma, pancreatic cancer,endometrial cancer, lung cancer, non-small cell lung cancer (NSCLC),gastric cancer, colon cancer, perianal adenoma, or central nervoussystem cancer.

Triple negative breast cancer (TNBC) is a type of breast cancer lackingthe expression of the estrogen receptor (ER), progesterone receptor(PR), and HER2 receptor kinase. As such, TNBC lacks the hormone andkinase therapeutic targets used to treat other types of primary breastcancers. Correspondingly, chemotherapy is often the initialpharmacotherapy for TNBC. Interestingly, AR is often still expressed inTNBC and may offer a hormone targeted therapeutic alternative tochemotherapy. In ER-positive breast cancer, AR is a positive prognosticindicator as it is believed that activation of AR limits and/or opposesthe effects of the ER in breast tissue and tumors. However, in theabsence of ER, it is possible that AR actually supports the growth ofbreast cancer tumors. Though the role of AR is not fully understood inTNBC, we have evidence that certain TNBC's may be supported by androgenindependent activation of AR-SVs lacking the LBD or androgen-dependentactivation of AR full length. As such, enzalutamide and otherLBD-directed traditional AR antagonists would not he able to antagonizeAR-SVs in these TNBC's. However, SARDs of this invention which arecapable of destroying AR-SVs (see Table 1 and Example 5) through abinding site in the NTD of AR (see Example 9) would be able toantagonize AR including AR-SV observed in TNBC patient derivedxenograpfts and provide an anti-tumor effect, as shown in Example 8.

Traditional antiandrogens such as bicalutamide and flutamide wereapproved for use in prostate cancer. Subsequent studies havedemonstrated the utility of antiandrogens (e.g., flutamide,spironolactone, cyproterone acetate, finasteride and chlormadinoneacetate) in androgen-dependent dermatological conditions such asandrogenic alopecia (male pattern baldness), acne vulgaris, andhirsutism (e.g., in female facial hair). Prepubertal castration preventssebum production and androgenic alopecia but this can be reversed by useof testosterone, suggesting its androgen-dependence.

The AR gene has a polymorphism of glutamine repeats (polyQ) within exon1 which when shortened may augment AR transactivation (i.e.,hyperandrogenism). It has been found that shortened polyQ polymorphismsare more common in people with alopecia, hirsutism, and acne. Classicantiandrogens are undesirable for these purposes because they areineffective through dermal dosing and their long-term systemic useraises the risks of untoward sexual effects such as gynecomastia andimpotence. Further, similar to CPRC discussed above, inhibition ofligand-dependent AR activity alone may not be sufficient as AR can beactivated by various cellular factors other than the endogeneousandrogens testosterone (T) and dihydrotestosterone (DHT), such as growthfactors, kinases, co-activator overexpression and/or promiscuousactivation by other hormones (e.g., estrogens or glucocorticoids).Consequently, blocking the binding of T and DHT to AR with a classicalantiandrogen may not be sufficient to have the desired efficacy.

An emerging concept is the topical application of a SARD to destroy theAR locally to the affected areas of the skin or other tissue withoutexerting any systemic antiandrogenism. For this use, a SARD that doesnot penetrate the skin or is rapidly metabolized would he preferrable.

Supporting this approach is the observation that cutaneous wound healinghas been demonstrated to he suppressed by androgens. Castration of miceaccelerates cutaneous wound healing while attenuating the inflammationin the wounds. The negative correlation between androgen levels andcutaneous healing and inflammation, in part, explains another mechanismby which high levels of endogenous androgens exacerbate hyperandrogenicdermatological conditions. Further, it provides a rationale for thetreatment of wounds such as diabetic ulcers or even trauma, or skindisorders with an inflammatory component such as acne or psoriasis, witha topical SARD.

Androgenic alopecia occurs in 50% of Caucasian males by midlife and upto 90% by 80 years old. Minoxidil (a topical vasodilator) andfinasteride (a systemic 5alpha reductase type 11 inhibitor) are FDAapproved for alopecia but require 4-12 months of treatment to produce atherapeutic effect and only arrest hair loss in most with mild tomoderate hair regrowth in 30-60%. Since currently available treatmentshave slow and limited efficacy that varies widely between individuals,and produce unwanted sexual side effects, it is important to find anovel approach to treat androgenic alopecia and other hyperandrogenicdermatologic diseases.

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative diseasecharacterized by selective loss of upper and lower motor neurons andskeletal muscle atrophy. Epidemiologic and experimental evidence suggestthe involvement of androgens in ALS pathogenesis (“Anabolic/androgenicsteroid nandrolone exacerbates gene expression modifications induced bymutant SOD1 in muscles of mice models of amyotrophic lateral sclerosis.”Galbiati M. Onesto E, Zito A, Crippa V, Rusmini P, Mariotti R,Bentivoglio M, Bendotti C, Poletti A. Pharmacol. Res. 2012, 65(2),221-230), but the mechanism through which androgens modify the ALSphenotype is unknown. A transgenic animal model of ALS demonstratedimproved survival upon surgical castration (i.e., androgen ablation).Treatment of these castrated animals with the androgen agonistnandrolone decanoate worsened disease manifestations. Castration reducesthe AR level, which may he the reason for extended survival. Thesurvival benefit is reversed by androgen agonist (“Androgens affectmuscle, motor neuron, and survival in a mouse model of SOD1-relatedamyotrophic lateral sclerosis.” Aggarwal T, Polanco M J, Scaramuzzino C,Rocchi A, Milioto C, Emionite L, Ognio E, Sambataro F, Galbiati M,Poletti A, Pennuto M. Neurobiol. Aging, 2014 35(8), 1929-1938). Notably,stimulation with nandrolone decanoate promoted the recruitment ofendogenous androgen receptor into biochemical complexes that wereinsoluble in sodium dodecyl sulfate, a finding consistent with proteinaggregation. Overall, these results shed light on the role of androgensas modifiers of ALS pathogenesis via dysregulation of androgen receptorhomeostasis. Antiandrogens should block the effects of nandroloneundecanoate or endogeneous androgens and reverse the toxicities due toAR aggegregation. Further, an antiandrogen that can block action ofLBD-dependent AR agonists and concomitantly lower AR protein levels,such as the SARDs of this invention, would be therapeutic in ALS.Riluzole is an available drug for ALS treatment, however, it onlyprovides short-term effects. There is an urgent need for drugs thatextend the survival of ALS patients.

Androgen receptor action promotes uterine proliferation.Hyperandrogenicity of the short polyQ AR has been associated withincreased leiomyoma or uterine fibroids. (Hsieh Y Y, Chang C C, Tsai FJ, Lin C C, Yeh L S, Peng C T. J. Assist. Reprod. Genet. 2004, 21),453-457). A separate study of Brazilian women found that shorter andlonger [CAG](n) repeat alleles of AR were exclusive to the leiomyomagroup in their study (Rosa F E, Canevari Rde A, Ambrosio E P, RamosCirilo P D, Pontes A, Rainho C A, Rogatto S R. Clin. Chem. Lab. Med.2008, 46(6), 814-823). Similarly, in Asian Indian women long polyQ ARwas associated with endometriosis and leiomyoma and can be regarded ashigh-risk markers. SARDs could he used in women with uterine fibroids,especially those expressing shorter and longer [CAG](n) repeat alleles,to treat existing uterine Fibroids, prevent worsening of fibroids and/orameliorate carcinogenicity associated with fibroids.

An abdominal aortic aneurysm (AAA) is an enlarged area in the lower partof the aorta, the major blood vessel that supplies blood to the body.The aorta, about the thickness of a garden hose, runs from your heartthrough the center of your chest and abdomen. Because the aorta is thebody's main supplier of blood, a ruptured abdominal aortic aneurysm cancause life-threatening bleeding. Depending on the size and the rate atwhich your abdominal aortic aneurysm is growing, treatment may vary fromwatchful waiting to emergency surgery. Once an abdominal aortic aneurysmis found, doctors will closely monitor it so that surgery can be plannedif it is necessary. Emergency surgery for a ruptured abdominal aorticaneurysm can he risky. AR blockade (pharmacologic or genetic) reducesAAA. Davis el al. (Davis J P, Salmon M, Pope N H, Lu G, Su G, Meher A,Ailawadi G, Upchurch G R Jr. 7 Vasc Surg (2016) 63(6):1602-1612) showedthat flutamide (50 mg/kg) or ketoconazole (150 mg/kg) attenuated porcinepancreatic elastase (0.35 U/mL) induced AAA by 84.2% and 91.5% comparedto vehicle (121%). Further AR -I- mice showed attenuated AAA growth(64.4%) compared to wildtype (both treated with elastase).Correspondingly, administration of a SARD to a patient suffering from anAAA may help reverse, treat or delay progression of AAA to the pointwhere surgery is needed.

X-linked spinal-bulbar muscular atrophy (SBMA—also known as Kennedy'sdisease) is a muscular atrophy that arises from a defect in the androgenreceptor gene on the X chromosome. Proximal limb and bulbar muscleweakness results in physical limitations including dependence on awheelchair in some cases. The mutation results in a protractedpolyglutamine tract added to the N-terminal domain of the androgenreceptor (polyQ AR). Binding and activation of this lengthened polyQ ARby endogeneous androgens (testosterone and DHT) results in unfolding andnuclear translocation of the mutant androgen receptor. Theandrogen-induced toxicity and androgen-dependent nuclear accumulation ofpolyQ AR protein seems to he central to the pathogenesis. Therefore, theinhibition of the androgen-activated polyQ AR might be a therapeuticoption (A. Baniahmad. Inhibition of the androgen receptor byantiandrogens in spinobulbar muscle atrophy. J. Mol. Neurosci. 201658(3), 343-347). These steps are required for pathogenesis and result inpartial loss of transactivation function (i.e., an androgeninsensitivity) and a poorly understood neuromuscular degeneration.Support of use antiandrogen comes in a report in which the antiandrogenflutamide protects male mice from androgen-dependent toxicity in threemodels of spinal bulbar muscular atrophy (Renier K J, Troxell-Smith S M,Johansen J A, Katsuno M, Adachi H, Sobue G, Chua J P, Sun Kim H,Lieberman A P, Breedlove S M, Jordan C L. Endocrinology 2014, 155(7),2624-2634). Currently there are no disease-modifying treatments butrather only symptom directed treatments. Efforts to target the polyQ ARof Kennedy's disease as the proximal mediator of toxicity by harnessingcellular machinery to promote its degradation, i.e., through the use ofa SARD, hold promise for therapeutic intervention. Selective androgenreceptor degraders such as those reported herein bind to and degrade allandrogen receptors tested (full length, splice variant, antiandrogenresistance mutants, etc.) so degradation of polyQ AR polymorphism isalso expected, indicating that they are promising leads for treatment ofSBMA.

Here we describe, infer alia, pyrrole, pyrazole, triazole, imidazole,and morpholine based selective androgen receptor degrader (SARD)compounds that may bind to the LBD and/or an alternate binding anddegradation domain (BDD) located in the NTD, antagonize AR, and degradeAR thereby blocking ligand-dependent and ligand-independent ARactivities. This novel mechanism produces improved efficacy when dosedsystemically (e.g., for prostate cancer) or topically (e.g.,dermatological diseases).

SUMMARY OF THE INVENTION

In one aspect, this invention provides a method of treating an androgenreceptor dependent disease or condition in a subject in need thereof,comprising administering to the subject a therapeutically effectiveamount of a selective androgen receptor degrader (SARD) compoundrepresented by the structure of formula I

wherein

-   -   T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;    -   R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;    -   or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;    -   Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;    -   Z is H, NOD, CN, halide, COON, COR, NHCOR, CONHR,    -   or Y and Z form a 5 to 8 membered fused ring;    -   X is CH or N;    -   R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃,        CH₂Cl, CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;    -   A is R² or R³;    -   R² is a live or six-membered saturated or unsaturated ring        having at least one nitrogen atom and 0, 1, or 2 double bonds,        optionally substituted with at least one of Q¹, Q², Q³ and Q⁴,        each independently selected from hydrogen, keto, substituted or        unsubstituted linear or branched alkyl, substituted or        unsubstituted cycloalkyl, substituted or unsubstituted        heterocycloalkyl, haloalkyl, CF₃, substituted or unsubstituted        aryl, substituted or unsubstituted phenyl, F, Cl, Br, I, CN,        NO₂, hydroxyl, alkoxy, OR, benzyl, NCS, maleimide, NHCOOR,        N(R)₂, NHCOR, CONHR, COOR or COR;    -   R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴,        OCOR⁴, OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴),        CON(R⁴)₂, SR⁴, SO₂R⁴, SOR⁴ SOH, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂,        NH₂, NH(R⁴), N(R⁴)₂, CO(N-heterocycle). NO₂, cyanate,        isocyanate, thiocyanate, isothiocyanate, mesylate, tosylate,        triflate, PO(OH)₂ or OPO(OH)₂; and    -   R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl,        wherein said alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl        groups are optionally substituted;    -   or its optical isomer or a racemic mixture thereof, isomer,        pharmaceutically acceptable salt, pharmaceutical product,        hydrate or any combination thereof.

In one embodiment, this invention provides a method of treating anandrogen receptor dependent disease or condition in a subject in needthereof, comprising administering to the subject a therapeuticallyeffective amount of a selective androgen receptor degrader (SARD)compound wherein the SARD compound is represented by the structure offormula IA:

wherein T, R¹, Y, Z, X, and A are as described in the compound offormula I, or its isomer, pharmaceutically acceptable salt,pharmaceutical product, hydrate or any combination thereof.

In one aspect, this invention provides a method of treating an androgenreceptor dependent disease or condition in a subject in need thereof,comprising administering to the subject a therapeutically effectiveamount of a selective androgen receptor degrader (SARD) compound whereinthe SARD compound is represented by the structure of formula IB:

wherein T, R¹, Y, Z, X, and A are as described in the compound offormula I, or its isomer, pharmaceutically acceptable salt,pharmaceutical product, hydrate or any combination thereof.

In one embodiment, this invention provides a method of treating anandrogen receptor dependent disease or condition in a subject in needthereof, comprising administering to the subject a therapeuticallyeffective amount of a selective androgen receptor degrader (SARD)compound wherein the SARD compound is represented by the structure offormula II:

wherein

-   -   T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;    -   R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;    -   or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;    -   Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;    -   Z is H, NOD, CN, halide, COOH, COR, NHCOR, CONHR,    -   or Y and Z form a 5 to 8 membered fused ring;    -   X is CH or N;    -   R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃,        CH₂Cl, CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;    -   A is R² or R³    -   R² is a pyrrole, pyrrolidine, pyrazole, pyrazolidine, triazole.        or morpholine ring, said ring optionally substituted with at        least one of Q¹, Q², Q³ and Q⁴, each independently selected from        hydrogen, keto, substituted or unsubstituted linear or branched        alkyl, substituted or unsubstituted cycloalkyl, substituted or        unsubstituted heterocycloalkyl, haloalkyl, CF₃, substituted or        unsubstituted aryl, substituted or unsubstituted phenyl, F, Cl,        Br, I, CN, NO₂, hydroxyl, alkoxy, OR, benzyl, NCS, maleimide,        NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR;    -   R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴,        OCOR⁴, OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴),        CON(R⁴)₂, SR⁴, SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂,        NH₂, NH(R⁴), N(R⁴)₂, CO(N-heterocycle), NO², cyanate,        isocyanate, thiocyanate, isothiocyanate, mesylate, tosylate,        triflate, PO(OH)₂ or OPO(OH)₂; and    -   R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl,        wherein said alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl        groups are optionally substituted;    -   or its optical isomer or a racemic mixture thereof, isomer,        pharmaceutically acceptable salt, pharmaceutical product,        hydrate or any combination thereof.

In one embodiment of the method of this invention, the SARD compound isrepresented by the structure of formula IIA:

wherein T, R¹, Y, Z, X, and A are as described in the compound offormula II, or its isomer, pharmaceutically acceptable salt,pharmaceutical product, hydrate or any combination thereof.

In one embodiment of the method of this invention, the SARD compound isrepresented by the structure of formula IIB:

wherein T, R¹, Y, Z, X, and A are as described in the compound offormula II, or its isomer, pharmaceutically acceptable salt,pharmaceutical product, hydrate or any combination thereof.

In one embodiment of the method of this invention, the SARD compound isrepresented by the structure of formula VII:

wherein

-   -   X is CH or N;    -   Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;    -   Z is H, NOD, CN, halide, COOH, COR, NHCOR, CONHR, or Y and Z        form a 5 to 8 membered fused ring;    -   R¹ is H, CH₃, CH₂F, CNH₂, CF₃, CH₂CH₃, or CF₂CF₃;    -   T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;    -   or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;    -   R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃,        CH₂Cl, CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; and    -   Q², Q³ and Q⁴ are each independently selected from hydrogen,        keto, substituted or unsubstituted linear or branched alkyl,        substituted or unsubstituted cycloalkyl, substituted or        unsubstituted heterocycloalkyl, haloalkyl, CF), substituted or        unsubstituted aryl, substituted or unsubstituted phenyl, F, Cl,        Br, I, CN, NO₂, hydroxyl, alkoxy, OR, arylalkyl, NCS, NHCOOR,        N(R)₂, NHCOR, CONHR, COOR or COR; or its optical isomer or a        racemic mixture thereof, isomer, pharmaceutically acceptable        salt, pharmaceutical product, hydrate or any combination        thereof.

In one embodiment of the method of this invention, the SARD compound isrepresented by the structure of formula VIIA:

wherein T, R¹, Y, Z, X, Q², Q³, and Q⁴ are as described in the compoundof formula VII, or its isomer, pharmaceutically acceptable salt,pharmaceutical product, hydrate or any combination thereof.

In one embodiment of the method of this invention, the SARD compound isrepresented by the structure of formula VIIB:

wherein T, R¹, Y, Z, X, Q², Q³, and Q⁴ are as described in the compoundof formula VII, or its isomer, pharmaceutically acceptable salt,pharmaceutical product, hydrate or any combination thereof.

In one embodiment of the method of this invention, in the compounds offormulas I, IA, IB, IIA, and/or IIB, Q¹, Q², Q³ and/or Q⁴ is hydrogen,CN, NO₂, CF₃, F, Cl, Br, I, NHCOOR, N(R)₂, NHCOR, COR, alkyl, alkoxy, orsubstituted or unsubstituted phenyl.

In one embodiment of the method of this invention, the SARD compound isrepresented by the structure of any one of the following compounds:

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention responds to at least one of: 1)AR-splice variant (AR-SV) degradation activity, 2) full length (AR-FL)degradation activity, 3) AR-SV inhibitory, or 4) AR-FL inhibitoryactivity.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is breast cancer.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is breast cancer that is AR expressingbreast cancer, AR-SV expressing breast cancer, and/or AR-V7 expressingbreast cancer.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is Kennedy's disease.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is acne.

In one aspect of this embodiment, the androgen receptor dependentdisease or condition in the method of this invention is acne vulgaris.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is overproduction of sebum.

In one aspect of this embodiment, reducing the overproduction of sebumtreats at least one of seborrhea, seborrheic dermatitis, or acne.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is hirsutism or alopecia.

In one aspect of this embodiment, the alopecia of the method of thisinvention is at least one of androgenic alopecia, alopecia areata,alopecia secondary to chemotherapy, alopecia secondary to radiationtherapy, alopecia induced by scarring, or alopecia induced by stress.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is a hormonal disease or condition in afemale.

In one embodiment, the hormonal disease or condition in a female of themethod of this invention is at least one of precocious puberty,dysmenorrhea, amenorrhea, multilocular uterus syndrome, endometriosis,hysteromyoma, abnormal uterine bleeding, early menarche, fibrocysticbreast disease, fibroids of the uterus, ovarian cysts, polycystic ovarysyndrome, pre-eclampsia, eclampsia of pregnancy, preterm labor,premenstrual syndrome, or vaginal dryness.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is a hormonal disease or condition in amale.

In one embodiment, the hormonal disease or condition in a male of themethod of this invention is at least one of hypergonadism,hypersexuality, sexual dysfunction, gynecomastia, precocious puberty ina male, alterations in cognition and mood, depression, hair loss,hyperandrogenic dermatological disorders, pre-cancerous lesions of theprostate, benign prostate hyperplasia, prostate cancer and/or otherandrogen-dependent cancers.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is sexual perversion, hypersexuality, orparaphilias.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is androgen psychosis.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is virilization.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is androgen insensitivity syndrome.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is cancer. In one embodiment, the canceris an AR-expressing cancer.

In one embodiment, the AR-expressing cancer of the method of thisinvention is at least one of breast cancer, testicular cancer, cancersassociated with partial androgen insensitivity syndromes (PAIS) such asgonadal tumors and seminoma, uterine cancer, ovarian cancer, cancer ofthe fallopian tubes or peritoneum, salivary gland cancer, bladdercancer, urogenital cancer, brain cancer, skin cancer, lymphoma, mantlecell lymphoma, liver cancer, hepatocellular carcinoma, renal cancer,renal cell carcinoma, osteosarcoma, pancreatic cancer, endometrialcancer, lung cancer, non-small cell lung cancer (NSCLC), gastric cancer,colon cancer. perianal adenoma, or central nervous system cancer.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is amyotrophic lateral sclerosis (ALS).

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is uterine fibroids.

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is abdominal aortic aneurysm (AAA).

In one embodiment, the androgen receptor dependent disease or conditionin the method of this invention is caused by polyglutamine (polyQ) ARpolymorphs.

In one aspect of this embodiment, the polyQ-AR of the method of thisinvention is a short polyQ polymorph or a long polyQ polymorph. In oneaspect of this embodiment, the polyQ-AR of the method is a short polyQpolymorph and the method further treats dermal disease.

In one aspect of this embodiment, the dermal disease of the method ofthis invention is at least one of alopecia, seborrhea, seborrheicdermatitis, or acne. In one aspect of this embodiment, the polyQ-AR ofthe invention is a long polyQ polymorph and the method further treatsKennedy's disease.

In one aspect, this invention provides a radioactively labeled SARDcompound represented by the structure of formula I:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

A is R² or ³;

R² is a five or six-membered saturated or unsaturated ring having atleast one nitrogen atom and 0, 1, or 2 double bonds, optionallysubstituted with at least one of Q¹, Q², Q³ and Q⁴, each independentlyselected from hydrogen, keto, substituted or unsubstituted linear orbranched alkyl, substituted or unsubstituted cycloalkyl, substituted orunsubstitutai heterocycloalkyl, haloalkyl, CF₃, substituted orunsubstituted aryl, substituted or unsubstitutai phenyl, F, Cl, Br, I,CN, NO₂, hydroxyl, alkoxy, OR, benzyl, NCS, maleimide, NHCOOR, N(R)₂,NHCOR, CONHR, COOR or COR;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate. thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted;

or its optical isomer or a racemic mixture thereof, isomer,pharmaceutically acceptable salt, pharmaceutical product hydrate or anycombination thereof;

wherein at least one of the protons of formula I is replaced by atritium atom.

In one embodiment, the radioactively labeled compound is represented bythe structure of ³H-1002:

wherein T is tritium (³H).

In one embodiment this invention provides an assay for observing andquantitating competitive NTD binding of a candidate NTD bindingcompound. wherein said assay comprises a compound of formula I, whereinat least one of the protons of the compound of formula I is replaced bya tritium atom. In another embodiment, the compound is ³H-1002(initiated 1002).

BRIEF DESCRIPTION OF THE DRAWINGS

The subject matter regarded as the invention is particularly pointed outand distinctly claimed in the concluding portion of the specification.The invention, however, both as to organization and method of operation,together with objects, features, and advantages thereof, may best beunderstood by reference to the following detailed description when readwith the accompanying drawings.

FIGS. 1A-1C: The transactivation result of 1002 was reported based onmeasured luciferase light emissions and reported as relative light unitintensity (RLU). FIG. 1A plotted the results with RLU reported on they-axis and SARD concentration on the x-axis, where the antagonist modewas reported in closed dots. A curve was fitted to the closed dots. FIG.1B illustrates the Western blot of the androgen receptor degradationassay with AD1 cells and the results were reported in Table 1, underSARD Activity: Full Length % Inhibition. FIG. 1C illustrates the Westernblot of the androgen receptor degradation splice variant assay withD567es cells. (The results in 22RV1 cells were reported in Table 1,under ‘SARD Activity: S.V. % Inhibition’.)

FIG. 2A and FIG. 2B: The transactivation results for 11 (an indole) and1002 (a pyrazole of this invention) were reported based on measuredluciferase light emissions and reported as relative light unit intensity(RLU). FIG. 2A plotted the results with RLU reported on the y-axis andSARD concentration on the x-axis, where the antagonist mode was reportedfor 11 and 1002. Compound 11 is represented in closed dots and solidline and 1002 is represented in open dots and dashed line. A curve wasfitted to the open and closed dots for 1002 and 11, respectively. FIG.2B illustrates the Western blots of an AR degradation assay with ADIcells (Full Length AR) and a splice variant assay with 22RV1 cells for11.118 (R-isomer of 11), 1002, and 1020 (R-isomer of 1002). The resultswere reported in Table I in columns labeled ‘SARD Activity: Full Length% Inhibition’ and ‘SARD Activity: S.V. % Inhibition’, respectively. Inshort, the R-isomer of indole and pyrazole SARDs retained SARD activity,in contrast to LBD-dependent inhibitors.

FIG. 3A and FIG. 3B: The transactivation result of 1003 was reportedbased on measured luciferase light emissions and reported as relativelight unit intensity (RLU). FIG. 3A plotted the results with RLUreported on the y-axis and SARD concentration on the x-axis, where theagonist mode was reported in closed dots and the antagonist mode wasreported in open dots. A curve was fitted to the open dots. FIG. 3Billustrates the Western blot of the full length androgen receptordegradation assay and the results were reported in Table 1, under SARDActivity: Full Length % Inhibition.

FIG. 4A and FIG. 4B: The transactivation result of 1004 was reportedbased on measured luciferase light emissions and reported as relativelight unit intensity (RLU). FIG. 4A plotted the results with RLUreported on the y-axis and SARD concentration on the x-axis, where theagonist mode was reported in closed dots and antagonist mode wasreported in open dots. A curve was fitted to the open dots. FIG. 4Billustrates the Western blot of the full length androgen receptordegradation assay and the results were reported in Table 1, under SARDActivity: Full Length % Inhibition. The numbers under the Western blotindicate the ratio of AR to actin in each lane.

FIG. 5A and FIG. 5B: The transactivation results of 1005 were reportedbased on measured luciferase light emissions and reported as relativelight unit intensity (RLU). FIG. 5A plotted the results with RLUreported on the y-axis and SARD concentration on the x-axis, where theagonist mode was reported in closed dots and antagonist mode wasreported in open. A curve was fitted to the open dots. FIG. 5Billustrates the Western blot of the full length androgen receptordegradation assay and the results were reported in Table 1, under SARDActivity: Full Length % Inhibition.

FIG. 6A and FIG. 6B: The transactivation result of 1006 was reportedbased on measured luciferase light emissions and reported as relativelight unit intensity (RLU). FIG. 6A plotted the results with RLUreported on the y-axis and SARD concentration on the x-axis, where theagonist mode was reported in closed dots and antagonist mode wasreported in open dots. A curve was fitted to the open dots. FIG. 6Billustrates the Western blot of the full length androgen receptordegradation assay and the results were reported in Table 1, under SARDActivity: Full Length % Inhibition.

FIG. 7: The Western blot of the full length androgen receptordegradation assay is shown for compound 17 and the results are reportedin Table 1, under SARD Activity: Full Length % Inhibition.

FIG. 8: The transactivation result of 1011 was reported based onmeasured luciferase light emissions and reported as relative light unitintensity (RLU). FIG. 8 plotted the results with RLU reported on they-axis and SARD concentration on the x-axis, where the antagonist modewas reported in closed dots. A curve was fitted to the closed dots.

FIG. 9: The transactivation result of 1010 was reported based onmeasured luciferase light emissions and reported as relative light unitintensity (RLU). FIG. 9 plotted the results with RLU reported on they-axis and SARD concentration on the x-axis, where the antagonist modewas reported in closed dots. A curve was fitted to the closed dots.

FIG. 10: The transactivation result of 1009 was reported based onmeasured luciferase light emissions and reported as relative light unitintensity (RLU). FIG. 10 plotted the results with RLU reported on they-axis and SARD concentration on the x-axis, where the antagonist modewas reported in closed dots. A curve was fitted to the closed dots.

FIG. 11: The transactivation result of 1008 was reported based onmeasured luciferase light emissions and reported as relative light unitintensity (RLU). FIG. 11 plotted the results with RLU reported on they-axis and SARD concentration on the x-axis, where the antagonist modewas reported in closed dots. A curve was fitted to the closed dots.

FIG. 12: The transactivation result of 1007 was reported based onmeasured luciferase light emissions and reported as relative light unitintensity (RLU). FIG. 12 plotted the results with RLU reported on they-axis and SARD concentration on the x-axis, where the antagonist modewas reported in closed dots. A curve was fitted to the closed dots.

FIGS. 13A-13C: The transactivation result of 1001 was reported based onmeasured luciferase light emissions and reported as relative light unitintensity (RLU). FIG. 13A plotted the results with RLU reported on they-axis and SARD concentration on the x-axis, where the antagonist modewas reported in closed dots. A curve was fitted to the closed dots. FIG.13B illustrates the Western blot of the full length androgen receptordegradation assay and the results were reported in Table 1, under SARDActivity: Full Length % Inhibition. FIG. 13C illustrates the Westernblot of the androgen receptor degradation splice variant assay with22RV1 cells and the results were reported in Table 1, under SARDActivity: S.V. % Inhibition.

FIG. 14: FIG. 14 illustrates the phase I and phase I & II data as a rawdata table for the determination of metabolic stability for 1002 inmouse liver microsomes (MLM) and the T_(1/2) (half-life in minutes) andCL_(int) (clearance in μL/min/mg protein) values calculated therefrom.

FIG. 15A and FIG. 15B: FIG. 15A reports phase I data as a raw data tableand graphed data for one experiment for 1002 in mouse liver microsomes(MLM). FIG. 15B reports phase I & II data as a raw data table andgraphed data for one experiment for 1002 in mouse liver microsomes(MLM). Value for T_(1/2) was 224 min. CL_(int) was 3.12 μL/min/mg.

FIG. 16A and FIG. 16B: FIG. 16A reports phase I data for human livermicrosomes (HLM). FIG. 16B reports phase I & II data as a raw data tableand graphed data for one experiment for 1002 in human liver microsomes(HLM). For this experiment, the calculated value for T_(1/2) wasinfinity and CL_(int) was 0. Suggesting greater stability for 1002 inHLM than MLM.

FIG. 17: FIG. 17 reports phase I data as a raw data table and grapheddata for one experiment for 1001 in mouse liver microsomes (MLM). Valuefor T_(1/2) was 23.5 min and CL_(int) was 29.5 μL/min/mg. Results depictrelatively poor stability for 1001, but still an improvement compared to11.

FIG. 18A and FIG. 18B: Hershberger method (mice): Male mice (20-25 gramsbody weight; n=5-7/group) were either left intact (FIG. 18A) orcastrated (FIG. 18B) and treated as indicated in the figures for 13days. Treatment of castrated mice was initiated 3 days after castration.Mice were sacrificed on day 14 after treatment initiation and seminalvesicles were removed and weighed. Seminal vesicles weights were eitherrepresented as is or were normalized to body weight and represented.

FIG. 19A and FIG. 19B: Hershberger method (rat): FIG. 19A reportsweights organs in intact Sprague Dawley rats with body weights of165-180 grams treated daily with vehicle, 40 mg/kg 1002.60 mg/kg 1002.or 20 mg/kg enzalutamide orally. After 13 days of treatment, the ratswere sacrificed and the weights of prostate, seminal vesicles, andlevator ani were measured. FIG. 19B reports the same data as a %decrease from vehicle. Bottom right pane illustrates intact vs.castrated % organ weights for vehicle treated rats.

FIG. 20A and FIG. 20B: Degradation of full length and splice vuriant(AR-v567ES) androgen receptors (in vitro) for 1010, 1012, 1014, 1015,1016, 1017, 1019 and 1022: FIG. 20A illustrates for each compound theWestern blot of the full length androgen receptor degradation assay. Theresults were reported in Table 1, under SARD Activity: Full Length %Inhibition. FIG. 20B illustrates the Western blot of the androgenreceptor degradation splice variant assay with D567es.

FIG. 21A and FIG. 21B: Anti-tumor efficacy for 1002 in triple negativebreast cancer (TNBC) patient-derived xenograft (PDX) is presented inHBrt 1071 triple negative breast cancer (FIG. 21A) and in HBrt 1361triple negative breast cancer (FIG. 21B).

FIG. 22: depicts binding of 1002 to AF-1 region of the N-terminal domain(NTD) of the androgen receptor. ID and waterLogsy NMR experimentsdemonstrate that 1002 bandwidth are broadened in the presence of apeptide derived from the AF-1 region of the NTD. Moreover, relaxationand waterLogsy demonstrate that the tumbling rate in solution for 1002is slowed upon addition of AF-1, strongly suggestive of 1002 binding toAF-1 region as its targeted protein interaction.

FIG. 23: depicts a LNCaP-enzalutamide resistant (LNCaP-EnzR) cells MR49Fgrowth assay using 1002 and 1014. 1002 and 1014 inhibit the growth ofLNCaP-EnzR cells in the low micromolar range.

FIG. 24: depicts the serum and tumor levels of 11, 34, 36, 96, 103,1002, 1010, 1012, and 1014 achieved in a 22RV1 xenograft experiment.

FIG. 25: depicts reductions in seminal vesicles weights (% change) foranimals treated with 34, 36, 1002, 1010, 1012, and 1014 in a Hershbergerassay.

FIG. 26: depicts tumor growth inhibition of LNCaP-enzalutamide-resistant(LNCaP-EnzR) xenografts treated with 1014 at 60 mg/kg administeredorally. Two different experiments (Experiment 1 and Experiment 2) areshown.

FIGS. 27A-27D: depict steady state fluorescence studies demonstratinginteractions between SARDs 1002, 1010, and 36 (indole), and N-terminalfragments of the AR such AR-NTD (amino acids 1-559) and AR-API (aminoacids 141-486). FIG. 27A depicts the perturbation of the fluorescentsignal of AR-NTD and AR-API in the presence of urea (denaturant). TMAO(folding stabilizer), and buffer, but no SARD. FIGS. 27B-27D depict theperturbations of AR-NTD and AR-AFI fluorescence associated with thetitrations of 1002 (FIG. 27B), 1010 (FIG. 27C), and 36 (FIG. 27D),respectively.

FIGS. 28A-28D: depicts degradation of full length and/or splice variant(22RV1) androgen receptors (in vitro) for 1024 (FIG. 28A), 1029 (FIG.28B), 1037 and 1041 (FIG. 28C), and 1044-1045 (FIG. 28D). FIGS. 28A,28C, and 28D illustrate the Western blots of the full length androgenreceptor degradation assay. The results were reported in Table 1, underSARD Activity: Full Length % Inhibition. FIG. 28B illustrates theWestern blots of the androgen receptor degradation splice variant assaywith 22RV1 cells which are represented in Table 1 in the column labeled‘SARD Activity: S.V. % Inhibition’.

FIGS. 29A-29C: depict that SARDs such as 1002 can antagonize F876L AR atdoses comparable to the wildtype AR and W741L AR at more potent dosesthan wildtype AR. (FIG. 29A) Enzalutamide inhibited F876L AR at dosesmore potent than wildtype AR but was a weaker antagonist of W741L AR(FIG. 29B). However, when the assay was run in agonist mode (FIG. 29C),enzalutamide, at higher doses acted as an agonist of F876L AR. This ischaracteristic of agonist switch mutations in which AR antagonists ofwildtype AR become AR agonists in due to the AR mutation. By comparison,SARDs like 1002 possess no intrinsic transcriptional agonist activity onwildtype AR or F876L AR, suggesting that tumors possessing agonistswitch mutations can be inhibited by SARDs of this invention. Similarly.W74IL is an agonist switch mutation conferring resistance tobicalutamide, which is inhibited by SARDs. FIG. 30E demonstrates thatSARDs of this invention can degrade F876L AR.

FIGS. 30A-30E: SARDs degrade the AR, AR-SV, and AR-F876L (MR49F), butnot PR and ER (see ZR-75-1 cells). FIG. 30A: LNCaP (compound 11); FIG.30B: LNCaP (compound 1002); FIG. 30C: ZR-75-1 (compound 1002); FIG. 30D:LNCaP-AR-V7 (compounds 11 and 1002); and FIG. 30E: MR49F (compound1002). LNCaP cells possess the T877A mutation which confers resistanceto flutamide (or hydroxyflutamide, the active metabolite) whichdemonstrates that SARDs will degrade an agonist switch mutant AR.Likewise, the F876L AR mutation confers resistance to enzalutamide andabiraterone and FIG. 30E demonstrates the ability to degrade thismutant. Cumulatively, this is good evidence that agonist switchmutations to current anti-androgens can be overcome with the SARDs ofthis invention.

FIGS. 31A and 31B: SARDs promote ubiquitination and require theproteasome to degrade the AR. FIG. 31A: compounds 11 and 1002; and FIG.31B: compound 1002 and bortezomib. The FIG. 31A shows an immunoblot inwhich a fusion portion with AR connected to hemagglutinin (HA) isexpressed in cells. Then the cells are treated with the indicated SARDsor untreated, the AR complex is immunoprecipitated with anti-IIA, andrun on a Western blot and visualized with anti-ubiquitin antibody(anti-Lib). In the untreated lane. there is no observed ubiquitinationof AR, whereas there is various degrees of ubiquitination of AR in theSARD (11 and 1002) treated lanes which are apparent as a smear of ARmolecular weights extending up from the fusion protein molecular weight.This indicated that the SARDs induced the ubiquitination of AR. RelativeAR levels are shown under each lane (10% input:AR). FIG. 31B indicatesthat 1002 degrades AR at 10 micromolar in the presence of 50 micromolarcycloheximide. Further, bortezimib, a protease inhibitor, does notinduce AR expression at 1, 5 and 10 micromolar. However. co-treatment ofcells with 1002 and 1, 5 and 10 micromolar resulted in a dose responsivereversal of the SARD activity of 1002. Reversal of SARD activity by aproteasome inhibitor indicates that the 1002 and other SARDs of thisinvention work by a proteasome-dependent protein degradation pathway.

FIG. 32: SARDs require AR-NTD containing constructs (e.g. AR or AGGchimera) to degrade the AR whereas SARDs were unable to degrade GR-NTDcontaining constructs (GR and GAA chimera).

FIGS. 33: SARDs inhibit the growth of enzalutamide-resistant VCaP CPRCxenografts in rats. The graph of tumor volume (TV) over time of VCaPCRPC in rats showed the ability of compound 1002 in rats (there is lessmetabolism of compound 1002 in rats than mice) to completely resolveVCaP xenografts (tumor volumes plotted as triangles) within 21 days,whereas enzalutamide only caused partial regression (tumor volumesplotted as squares). VCaP is an androgen-dependent CRPC cell line thatis partially sensitive to enzalutamide, but fully sensitive to SARDs ofthis invention. Cai et al. (PM ID: 21868758) have characterized VCaPcells as expressing high levels of androgen biosynthesis enzymes CYP17A1and AKR1C3 resulting in high intratumoral androgen levels andreactivation of the AR-axis. This model demonstrated that in the absenceof pharmacokinetic harriers (i.e., high levels of metabolism and/or poorabsorption and distribution in mice tumor xenograft models), that SARDscan lead to the complete resolution of castration resistant prostatecancers.

FIGS. 34A-34D: SARDs inhibit AR and Enz-R-AR function and cell growth.FIG. 34A: FKBPS expression in LNCaP cells; FIG. 34B: Growth inhibitionof LNCaP cells; FIG. 34C: FKBPS expression in enzalutamide resistant(EnzR)LNCaP cells; and FIG. 34D: Growth inhibition in LNCaP-EnzR cells.1002 inhibited the AR-dependent gene FKBPS in either LNCaP andLNCaP-EnzR cells demonstrating the ability to inhibit the AR-axis ineither CRPC's such as LNCaP (T877A) or enzalutamide resistant prostatecancers, and, correspondingly, to also inhibit cell growth in theseAR-dependent cell lines whereas enzalutamide was unable to significantlyinhibit FKBPS or growth in the LNCaP-EnzR cell line.

FIG. 35A: SARDs of this invention regressed the VCaP (enzalutamidesensitive) tumors grown in castrated rats to undetectable levels. FIG.35B shows tumor volume data for the individual animals in thisexperiment. Solid line is vehicle treated rats, larger dashes in theline are for enzalutamide treated rats, and smaller dashes are for 1002treated rats.

FIG. 36A: SARDs inhibited growth of tumor, caused rapid tumorregression, and rapidly reduced PSA serum to zero in a singlecryptorchid animal (i.e., androgen replete milieu) implanted with VCaPcells which were rendered enzalutamide resistant (MDVR). The left paneshows the tumor volume for this animal. The right pane show that 1002immediately and completely reduced PSA to zero, whereas enzalutamidetreated xenograft has only a modest PSA response. FIG. 36B: demonstratesthat vehicle treated and enzalutamide treated MDVR VCaP xenograftcontinued to grow rapidly. This established that the MDVR VCaP model wasa good model of enzalutamide resistance.

FIG. 37 demonstrates that the experiment, when repeated in multiple(N=3) intact (not cryptorchid) rats, again produces rapid and completetumor regression with SARD treatment but rapid growth with enzalutamidetreatment which was similar to vehicle.

FIG. 38 demonstrates that the SARD is able to fully inhibit MDVR VCaPtumors in castrated animals but did not regress the tumors asdramatically as in intact rats, whereas enzalutamide treated tumorsgrowth comparably to vehicle. The preference for intact in this modelwas an unexpected results never before reported anywhere to ourknowledge.

FIGS. 39A-39C demonstrate that 11 has poor metabolism and oralpharmacodynamic properties. FIG. 39A. 11 has no effect on seminalvesicles when administered orally. C57BL6 mice weighing 20-25 grams(n=5/group) were treated orally with vehicle (15% DMSO+85% PEG-300) orthe indicated doses of 11 or enzalutamide. Animals were sacrificed after14 days of treatment and weights of seminal vesicles were recorded andnormalized to body weight. The values are represented as percent changefrom vehicle-treated animals. * * * p<0.001. FIG. 39B. 11 has no effecton the growth of enzalutamide-resistant xenograft when administeredorally. Enzalutamide-resistant LNCaP cells (MR49F) were implantedsubcutaneously in nude mice. Once the tumors reached 100-200 mm³, theanimals were castrated and the tumors were allowed to develop ascastration-resistant tumors. Once the tumors reach 200-300 mm³, theanimals (n=8-10/group) were randomized and treated orally with vehicle(15% DMSO +85% PEG-300) or 100 mg/kg 11. Tumor volume was measured twiceweekly. FIG. 39C. 11 has poor metabolism properties. Liver microsomesfrom mouse (MLM) and human (HLM) were incubated with 11 as indicated inthe methods and the amount of compound present at different points wasidentified using LC-MS/MS method. Data from both phase I and IImetabolism are presented here. The data are represented as half-life(T_(1/2) (minutes)) and intrinsic clearance (Cl_(int)).

FIGS. 40A-40C demonstrate the structure and properties of 1002. FIG.40A. Structure of 1002. FIG. 40B left panel. 1002 does not hind to theAR-LSD. Purified GST-tagged AR-LSD protein was incubated for 16 hours at4° C. with a dose response (1 pM to 100 μM) of the indicated compoundsin the presence of 1 nM ³H mibolerone. Unbound ³H was washed and thebound ³H was counted using a scintillation counter. FIG. 40B rightpanel. COS7 cells were transfected with 50 ng of AR-LBD. Cells weretreated 48 hours after transfection with a dose response (1 pM to 10 μM)of the indicated compounds in the presence of 1 nM ³H mibolerone for 4hours. Unbound ³H mibolerone was washed with cold PBS and the bound ³Hwas eluted with ice cold ethanol. ³H was counted using a scintillationcounter. FIG. 40C. 1002 comparably inhibits the transactivation ofwildtype and mutant ARs. COS7 cells were transfected with 25 ng of cmvhAR, hAR F876L, or hAR W741L. 0.25 μg GRE-LUC, and 10 ng CMV-renilla LUCusing lipofectamine. Cells were treated 24 hours after transfection witha dose response of 1002 or enzalutamide in combination with 0.1 nM R1881(F876L agonist graph experiment was performed in the absence of 0.1 nMR1881) and luciferase assay was performed 48 hours after transfection.Firefly luciferase was divided by renilla luciferase. Values shown inthe graphs are IC₅₀ values. Experiments were performed at least n=3times and the representative graph is shown here. DHTdihydrotestosterone; AR-androgen receptor; LBD-Iigand binding domain;GST-glutathione S transferase.

FIG. 41A-41I: demonstrate that 1002 selectively degrades wildtype andenzalutamide-resistant ARs. FIG. 41A. 1002 destabilizes wildtype AR.LNCaP cells were maintained in charcoal-stripped serum-containing mediumfor 2 days. Cells were treated with the indicated doses of 1002 orenzalutamide (Enz) or bicalutamide (Bic) (right panel; enzalutamide andbicalutamide were used at 10 μM) in the presence of 0.1 nM R1881 for 24hours, protein was extracted, and Western blot for AR and actin wasperformed. Lower bar graph shows no effect of 1002 on AR mRNA expressionunder the same experimental conditions. FIG. 41B. 1002 destabilizesenzalutamide-resistant AR. Enzalutamide-resistant LNCaP cells (MR49F)were cultured and treated as indicated above for LNCaP cells. Westernblot for AR and actin was performed with the protein extracts. FIG. 41C.1002 selectively degrades the AR. T47D cells maintained in fullserum-containing medium were treated as indicated in the figure with1002. Twenty four hours after treatment, cells were harvested. proteinextracted, and Western blot for PR. ER, and actin was performed. FIG.41D. ZR-75-1 breast cancer cells were maintained in 1% csFBS-containingmedium for two days. Cells were treated as indicated in the figures for48 hours with cells retreated after 24 hours. Cells were harvested andWestern blot for AR, PR, ER, and GAPDH was performed. FIG. 41E. 1002destabilizes the AR. LNCaP cells cultured in full scrum-containingmedium were treated with 10 μM 1002, 50 μM cycloheximide, or combinationof 1002 and cycloheximide. Cells were harvested at the indicatedtime-points and Western blot for AR and GAPDH was performed. FIG. 41F,1002 promotes ubiquitination of the AR. COS7 cells were transfected with1 μg cmv hAR and HA-ubiquitin. Cells were treated 48 hours aftertransfection for 6 hours. Cells were harvested. protein extracted, andimmunoprecipitation for HA and Western blot for AR were performed. 10%of the protein extract was loaded as input. FIG. 41G. LNCaP cellsmaintained in 1% charcoal-stripped serum-containing medium for 2 dayswere treated with 1002 or 11 in the presence and absence of proteasomeinhibitor, MG-132 and HSP-90 inhibitor, 77AAG, for 6 hours.Immunoprecipitation for AR was performed with the protein extract andWestern blot with mono-and poly-ubiquitin antibody was performed. FIG.41H. 1002 degrades the AR by proteasome pathway. LNCaP cells plated ingrowth medium were treated as indicated in the figure for 8 hours.Western blot for AR and GAPDH was performed in the protein extracts.FIG. 41I. Known ubiquitin sites do not play a role in 1002-induceddegradation of the AR. COS7 cells were transfected with 1 μg of wildtypeAR or AR where three lysines (K311, K846, K848) were mutated to arginine(K to R). Cells were treated 24 hours after transfection for 24 hoursand Western blot for AR and GAPDH was performed. Experiments wereperformed at least n=3 and representative blots are shown here.AR-androgen receptor; PR-progesterone receptor; ER-estrogen receptor;IP-immunoprecipitation; IB-immunoblot (Western blot); HA-hemagglutinin;Ub-ubiquitin; cyclohex-cycloheximide-protein-synthesis inhibitor;Enz-enzalutamide; Bic-bicalutamide.

FIGS. 42A-42B demonstrates that1002 interacts with AR AF-1 domain. FIG.42A. Nuclear magnetic resonance (NMR). 1002 (250 μM) dissolved indeuterated DMSO (DMSO-d₆) was added to an NMR tube alone or incombination with 5 μM AF-1 purified protein. The intensity of nuclearspin was measured at different magnetic fields (8 ppm). The peaksbetween 7 and 8 correspond to the aromatic rings of 1002. FIG. 42B.Raman Spectroscopy. Raman spectra of 1002, AF-1 purified protein, andtheir mixtures is shown. Simulation of 1002 binding (trans conformation)to glycine. Binding energies of 1002 in trans conformation to differentamino acids.

FIGS. 43A-43C demonstrates that 1002 interacts with the activationfunction 1 (AF-1) domain of the AR. FIG. 43A. Steady state fluorescenceemission spectra for purified AR-AF1 or AR-NTD proteins. AR-AF-1 orAR-N-terminus domain (NTD) (1 μM) and 1002 were pre-incubated for atleast 30 minutes and steady state fluorescence was measured. Theemission spectra were all corrected to buffer alone as necessary. FIG.43B. ³H-1002 demonstrates binding to AR-NTD. HEK-293 cells weretransfected with the indicated plasmids. Protein was extracted andincubated with the indicated compounds. Bound radioactive ligands wereseparated from unbound radioactive nucleotides using G-25 Sephadexcolumns. The incorporated radioactivity was counted in scintillationcounter. FIG. 43C. Thermal shift assay. Thermal shift assay wasperformed in HEK-293 cells transfected with AR-NTD or AR-LBD asdescribed in the methods. AR-androgen receptor; NTD-N-terminus domain:AF-1-activation function-1 domain.

FIGS. 44A-44E demonstrate that AR N-terminus domain is sufficient for1002 to degrade the AR. FIG. 44A. Map of the constructs used in studiesto determine the domain important to degrade the AR. FIG. 44B. COS7cells were transfected with 2.5 μg of the indicated constructs andHA-ubiquitin. Cells were treated 24 hours after transfection andharvested 24 hours after treatment. Western blot for AR and GAPDH (leftpanel) and GR and GAPDH (right panel) was performed. Bottom: COS7 cellswere transfected with 2.5 μg of AR or AGG and HA-ubiquitin. Twenty-fourhours after transfection, cells were treated with vehicle or 10 μM 1002for 6 hours. Immunoprecipitation was performed with HA antibody andWestern blot was performed with AR antibody. 10% loading control isshown below. FIG. 44C. COS7 cells were transfected with 0.25 μg GRE-LUC,10 ng CMV-LUC, 25 ng of the respective receptor, and 0.25 μg HA-Ub.Cells were treated as indicated in the figure in combination with 0.1 nMR1881 or dexamethasone (Dex). Luciferase assay was performed 48 hoursafter treatment (n=3). *p<0.05. FIG. 44D. Tau-5 domain of the AR isimportant for 1002-dependent degradation of AR. COS7 cells weretransfected with 2.5 μg of the indicated constructs and HA-ubiquitin andWestern blot for AR using AR C19 antibody and GAPDH was performed(Right). HA-ubiquitin was immunoprecipitated and Western blot for AR wasperformed (Left). FIG. 44E. R-isomer (1020) and racemic mixture of 1002antagonize the AR comparably to the S-isomer of 1002. COS7 cells weretransfected with 0.25 μg GRE-LUC. 10 ng CMV-LUC, 25 ng cmv hAR. Cellswere treated with a dose response of the indicated compounds in thepresence of 0.1 nM R1881. Luciferase assay was performed 24 hours aftertreatment and firefly luciferase values were normalized to renillaluciferase. FIG. 44F. 1002 does not inhibit early induction of NDRG1 andMT2A pre-mRNAs. LNCaP cells maintained in charcoal-strippedserum-containing medium for 2 days were treated as indicated in thefigures in triplicates. Cells were pre-treated with 10 μM 1002 for 30minutes before treatment with 0.1 nM R1881. Cells were harvested, RNAisolated, and the expression of various pre-mRNAs was measured at theindicated time-points. All the experiments were repeated three times anda representative experiment is presented here. AR-androgen receptor;GR-glucocorticoid receptor; Ub-ubiquitin; dTau5-AR plasmid withtransactivation function-5 (Tau5) domain deleted; NTD-N terminus domain;DBD-DNA binding domain; Hin-Hinge; LBD-ligand binding domain;Dex-dexamethasone; AGG-AR NTD, GR DBD and LBD; GAA-GR NTD, AR DBD andLBD.

FIGS. 45A-45D demonstrate that 1002 degrades and inhibits AR-V7function. FIG. 45A. 1002 degrades AR-SV. LNCaP-AR-V7 cells (LNCaP cellsthat stably express doxycycline-inducible AR-V7; left panel) or LNCaP-95cells (middle panel) were maintained in charcoal-strippedserum-containing medium for 2 days. Doxycycline (10 ng/mL) was added tothe LNCaP-AR-V7 cells during this period to induce the AR-V7 synthesis.After two days, medium was changed and the cells were treated with theindicated doses of 1002 (11 was used as a positive control in the leftpanel) for 24 hours. Protein was extracted and Western blot for the ARand GAPDH was performed. Bar graph shows the lack of effect on AR-V7mRNA in the presence of 1002 under similar conditions. FIG. 45B. 1002inhibits AR-V7-regulated gene. LNCaP-AR-V7 cells were maintained incharcoal-stripped serum-containing medium for 2 days. Cells were treatedas indicated in the figure with 10 μM of the compounds in the presenceof 0.1 nM R1881 or 10 ng/mL doxycycline (cells were pre-treated with1002 for 30 minutes for combination with R1881 and for 24 hours forcombination with doxycycline). Twenty four hours after treatmentinitiation the cells were harvested. RNA isolated, and the expression ofFKBP5 or EDN2 was determined by realtime PCR. Gene expression valueswere normalized to the expression of GAPDH. *p<0.05. FIG. 45C. 1002inhibits recruitment of AR and AR-V7 to promoters of responsive genes.LNCaP-ARV7 cells were maintained in charcoal stripped serum-containingmedium for 2 days. Medium was changed and the cells were treated with 10μM 1002 or enzalutamide in the presence of 0.1 nM R1881 (AR ChIP) or 10ng/mL doxycycline (AR-V7 ChIP) for 6 hours (cells were pre-treated with1002 for 30 minutes). ChIP assay was performed with AR antibody or AR-V7antibody and real time PCR for the indicated DNA regions was performed.ChIP assays were performed at least three independent times and arepresentative experiment is shown here. FIG. 45D. 1002 inhibitsrecruitment of AR-V7 in 22RV1 cells. 22RV1 cells were maintained incharcoal stripped serum-containing medium for 2 days. Medium was changedand the cells were treated with 10 _(H)M 1002. or enzalutamide in thepresence of 0.1 nM R1881 for 6 hours (cells were pre-treated with 1002for 30 minutes). ChIP assay was performed with AR-V7 antibody and realtime PCR for the indicated DNA regions was performed. ChIP assays wereperformed at least three independent times and a representativeexperiment is shown here.

FIGS. 46A-46C demonstrate that 1002 inhibits wildtype AR andenzalutamide-resistant AR-dependent gene expression and prostate cancercell growth. FIG. 46A. 1002 inhibits the expression of AR-target genesin LNCaP cells. LNCaP cells maintained in charcoal-strippedserum-containing medium for 2 days were treated with a dose response of1002 or enzalutamide in the presence of 0.1 nM R1881. RNA was isolated24 hours after treatment and the expression of PSA (top panel) and FKBP5(middle panel) was quantified and normalized to GAPDH using real timePCR primers and probes. For the growth assay (bottom panel), cells weremaintained and treated as indicated above for the gene expressionstudies, but were treated for 6 days with medium change and retreatmentafter 3 days. Sulforhodamine B (SRB) assay was performed to determinethe number of viable cells. FIG. 46B. 1002 inhibits the expression ofAR-target genes in enzalutamide-resistant cells. Enzalutamide-resistantAR-expressing LNCaP cells (MR49F) were cultured and treated as indicatedin panel A. RNA was isolated and the expression of AR-target gene FKBP5(top panel) was measured and normalized to GAPDH using realtime PCRprimers and probe. Growth assay in MR49F cells was performed asindicated for LNCaP cells(bottom panel). FIG. 46C. Gene expression arrayin MR49F indicates 1002 completely reverses the expression of genesregulated by R1881. LNCaP cells were maintained in charcoal-strippedserum-containing medium for 2 days and treated with vehicle. 0.1 nMR1881 alone or in combination with 10 μM of 1002. RNA was isolated 24hours after treatment and hybridized to Clarion D microarray. Genes thatwere differentially expressed by 1.5-fold and q<0.05 in R1881-treatedsamples compared to vehicle-treated samples are expressed in the heatmapat the top. Bottom heatmap shows the pattern of genes that were notregulated by R1881 (n=3-4/group).

FIG. 47A-47B demonstrate that 1002 does not inhibit proliferation ofAR-negative cells. FIG. 47A. PC-3 cells were plated in 1%charcoal-stripped scrum-containing medium. Cells were treated with 1 or10 μM of 1002 in the presence 010.1 nM R1881. Cells were re-treatedthree days later and the number of viable cells was measured by celltiter glo assay. FIG. 47B. 1002 inhibits PSA expression and cellproliferation in enzalutamide-resistant VCaP (MDVR) cells. MDVR cellswere plated in 1% charcoal stripped serum-containing medium. Cells weretreated for 24 hours (left panel) or for 6 days (right panel).Expression of PSA was measured and normalized to GAPDH (left panel).Number of viable cells was measured by cell titer glo assay (rightpanel). *p<0.05. Enza-enzalutamide.

FIGS. 48A-48E demonstrate that 1002 has appropriate pharmacokinetic andpharmacodynamic properties. FIG. 48A-48B. 1002 is stable up to 24 hoursin rats. Sprague Dawley rats (n=3-6/group) were dosed once with theindicated doses of 1002 once (A) or for 7 days (B). Blood was collectedat the indicated time points on day 1 (A) or day 7 (B) and the amount of1002 remaining in the plasma was measured using LC-MS/MS method. FIG.48C. 1002 inhibits seminal vesicles weight in mice and prostate andseminal vesicles weight in rats. C57BL6 mice (top panel) weighing 20-25grams (n=5/group) or Sprague Dawley rats (middle and bottom) weighing200-250 grams (n=5/group) were treated orally with vehicle (15% DMS0+85%PEG-300) or the indicated doses of 1002 or enzalutamide. Animals weresacrificed after 14 days (top and middle) or after 4 days (bottom) oftreatment and weights of prostate and seminal vesicles were recorded andnormalized to body weight. The values are represented as percent changefrom vehicle-treated animals. FIG. 48D. 1002 penetrates and getsaccumulated in the tumors. Drug was extracted from serum and tumorsshown in FIG. 48E and 1002 was measured using LC-MS/MS (n=4/group). FIG.48E. 1002 inhibits proliferation and increases apoptosis. Formalin-fixedtumor samples from FIG. 48E were stained for Ki67 (top panel) and TUNEL(bottom panel). Percent stained cells were quantified using an automatedsoftware. Seminal vesicles weight normalized to body weight is expressedas percent change from vehicle control (FIG. 48F) *p<0.05; **p<0.01.mpk=mg/kg body weight. PK-pharmacokinetic; PD-pharmacodynamic.

FIG. 49A-49E demonstrate that 1002 inhibits the growth ofandrogen-dependent and enzalutamide-refractory castration-resistantprostate cancer xenografts. FIG. 49A. 1002 inhibits growth ofenzalutamide-resistant xenograft. Enzalutamide-resistant LNCaP cells(MR49F) were implanted subcutaneously in NSG mice. Once the tumorsreached 100-200 mm³, the animals were castrated and the tumors wereallowed to develop as castration-resistant tumors. Once the tumors reach200-300 mm³, the animals (n=8-10/group) were randomized and treatedorally with vehicle (15% DMSO+85% PEG-300) or the indicated doses of1002. Tumor volume was measured twice weekly. Animals were sacrificed onday 30 and tumor weights were recorded. Values arc represented asaverage ±S.E. *P<0.05; **P<0.01. FIG. 49B. 1002 regresses tumors inimmune-compromised rats. VCaP prostate cancer cells (10 million) weremixed with 50% matrigel implanted subcutaneously in SRGimmune-compromised rats. Once the tumors reached 1000-2000 mm³. theanimals were castrated and the tumors were allowed to regrow as CRPC.Once the tumors grew after castration to 2000 mm³. the animals wererandomized and treated orally with vehicle (DMSO+PEG-300 (15:85)), 30mg/kg enzalutamide, or 60 mg/kg 1002. Tumor volume was measured thriceweekly. Lines in the box indicate that the tumors in the treated groupsarc significantly different at p<0.01 to 0.001 from the vehicle group onthe respective days. FIG. 49C. 1002 regresses the growth ofenzalutamide-resistant VCaP tumors (MDVR). Tumor studies were conductedas indicated in panel B in SRG rats with MDVR enzalutamide-resistantVCaP cells. Western blot. Protein extracts from the tumors werefractionated on a SDS-PAGE and were Western blotted with AR and GAPDHantibodies. FIG. 49D. 1002 regresses tumors in intact SRG rats. MDVRcells (10 million) were implanted subcutaneously. Once the tumors reachabove 2000 mm³, the animals were randomized and treated orally withvehicle, 30 mg/kg enzalutamide, or 60 mg/kg 1002. Individual animal dataarc presented. Serum PSA was measured using ELISA in three rats (onefrom each group) and represented in the bottom right panel. Westernblots for AR and GAPDH are shown in the lower panel. FIG. 49E. 1002dose-dependently inhibits MDVR tumor growth in intact SRG rats.Xenograft studies were conducted in intact rats (n=5/group) as indicatedabove with a dose response of 1002. Tumor volume was measured thriceweekly. Lines in the box indicate that the tumors in the treated groupsare significantly different at p<0.01 to 0.001 from the vehicle group onthe respective days. Tumor weights and serum PSA were recorded at theend of the treatment period. Mpk-mg/kg body weight; Enza-enzalutamide.

FIGS. 50A-50C demonstrate that the synthesis of ³H-1002 produced aproduct that was pure by HPLC analysis (FIG. 50A) in which theradioactivity and UV absorption eluted at the same retention times asdetermined by HPLC using two different detectors (FIG. 50B); and massspectroscopic analysis indicated that the tritium was added as seen inthe 2 proton shift in m/z ratio (FIG. 50C) which possessed 16 Ci/mmol ofradioactivity. Taken together, this demonstrates successful synthesis of³H-1002.

It will be appreciated that for simplicity and clarity of illustration,elements shown in the figures have not necessarily been drawn to scale.For example, the dimensions of some of the elements may be exaggeratedrelative to other elements for clarity. Further, where consideredappropriate, reference numerals may be repeated among the figures toindicate corresponding or analogous elements.

DETAILED DESCRIPTION OF THE PRESENT INVENTION

In the following detailed description, numerous specific details are setforth in order to provide a thorough understanding of the invention.However. it will be understood by those skilled in the art that thepresent invention may be practiced without these specific details. Inother instances, well-known methods, procedures, and components have notbeen described in detail so as not to obscure the present invention.

Androgens act in cells by binding to the AR, a member of the steroidreceptor superfamily of transcription factors. As the growth andmaintenance of prostate cancer (PCa) is largely controlled bycirculating androgens, treatment of PCa heavily relies on therapies thattarget AR. Treatment with AR antagonists such as enzalutamide,bicalutamide or hydroxyflutamide to disrupt receptor activation has beensuccessfully used in the past to reduce PCa growth. All currentlyavailable AR antagonists competitively bind AR and recruit corepressorssuch as NCoR and SMRT to repress transcription of target genes. However,altered intracellular signaling, AR mutations, and increased expressionof coactivators lead to functional impairment of antagonists or eventransformation of antagonists into agonists. Studies have demonstratedthat mutation of W741 and T877 within AR converts bicalutamide andhydroxyflutamide, respectively, to agonists. Similarly, increasedintracellular cytokines recruit coactivators instead of corepressors toAR-responsive promoters subsequently converting bicalutamide to anagonist. Similarly, mutations that have been linked to enzalutamideresistance include F876. H874. T877, and di-mutants T877/S888,T877/D890, F876/T877 (i.e., MR49 cells), and H874/T877 (GenomeBiol.(2016) 17:10 (doi: 10.1186/s13059-015-0864-1)). Abirateroneresistance mutations include L702H mutations which results in activationof the AR by glucocorticoids such as prednisone, causing resistance toabiraterone because abiraterone is usually prescribed in combinationwith prednisone. If resistance develops to enzalutamide then often thepatient is refractory to abiraterone also and vice versa; or theduration of response is very short. This situation highlights the needfor a definitive androgen ablation therapy to prevent AR reactivation inadvanced prostate cancers.

Despite initial response to androgen deprivation therapy (ADT), PCadisease progression is inevitable and the cancer emerges ascastration-resistant prostate cancer (CRPC). The primary reason forcastration resistant prostate cancer (CRPC) re-emergence isre-activation of androgen receptor (AR) by alternate mechanisms such as:

-   -   (a) intracrine androgen synthesis;    -   (b) expression of AR splice variants (AR-SV), e.g., that lack        ligand binding domain (LSD);    -   (c) AR-LSD mutations with potential to resist antagonists;    -   (d) hyper-sensitization of AR to low androgen levels, e.g., due        to AR gene amplification or AR mutation;    -   (e) amplification of the AR gene within the tumor; and    -   (f) over expression of coactivators and/or altered intracellular        signal transduction.

The invention encompasses novel selective androgen receptor degrader(SARD) compounds encompassed by formula I, which inhibit the growth ofprostate cancer (PCa) cells and tumors that are dependent on AR fulllength (AR-FL) including pathogenic and resistance mutations andwildtype, and/or AR splice variants (AR-SV) for proliferation.

As used herein. unless otherwise defined, a “selective androgen receptordegrader” (SARD) compound is an androgen receptor antagonist capable ofinhibiting the growth of PCa cells and tumors that are dependent onAR-full length (AR-FL) and/or AR splice variants (AR-SV) forproliferation. The SARD compound may not hind to ligand binding domain(LBD). Alternatively, a “selective androgen receptor degrader” (SARD)compound is an androgen receptor antagonist capable of causingdegradation of a variety of pathogenic mutant variant AR's and wildtypeAR and hence are capable of exerting anti-androgenism is a wide varietyof pathogenic altered cellular environments found in the disease statesembodied in this invention. In one embodiment, the SARD is orallyactive. In another embodiment, the SARD is applied topically to the siteof action.

The SARD compound may hind to the N-terminal domain (NTD) of the AR; toan alternate binding and degradation domain (BDD) of the AR; to both theAR ligand binding domain (LBD) and to an alternate binding anddegradation domain (BDD); or to both the N-terminal domain (NTD) and tothe ligand binding domain (LBD) of the AR. In one embodiment, the BDDmay be located in the NTD. In one embodiment, the BDD is located in theAF- I region of the NTD. Alternatively, the SARD compound may be capableof: inhibiting growth driven by the N-terminal domain (NTD)-dependentconstitutively active AR-SV; or inhibiting the AR through binding to adomain that is distinct from the AR LBD. Also, the SARD compound may bea strong (i.e., highly potent and highly efficacious) selective androgenreceptor antagonist, which antagonizes the AR stronger than other knownAR antagonists (e.g., enzalutamide, bicalutamide and abiraterone).

The SARD compound may be a selective androgen receptor antagonist. whichtargets AR-SVs, which cannot be inhibited by conventional antagonists.The SARD compound may exhibit any one of several activities including,but not limited to: AR-SV degradation activity; AR-FL degradationactivity; AR-SV inhibitory activity (i.e., is an AR-SV antagonist);AR-FL inhibitory activity (i.e., is an AR-FL antagonist); inhibition ofthe constitutive activation of AR-SVs; or inhibition of the constitutiveactivation of AR-FLs. Alternatively, the SARD compound may possess dualAR-SV degradation and AR-SV inhibitory functions, and/or dual AR-FLdegradation and AR-FL inhibitory functions; or alternatively possess allfour of these activities.

The SARD compound may also degrade AR-FL and AR-SV. The SARD compoundmay degrade the AR through binding to a domain that is distinct from theAR LBD. The SARD compound may possess dual degradation and AR-SVinhibitory functions that are distinct from any available CRPCtherapeutics. The SARD compound may inhibit the re-activation of the ARby alternate mechanisms such as: intracrine androgen synthesis,expression of AR-SV that lack ligand binding domain (LBD) and AR-LBDmutations with potential to resist antagonists, or inhibit re-activatedandrogen receptors present in pathogenic altered cellular environments.

Examples of AR-splice variants include, but are not limited to, AR-V7and ARv567es (a.k.a. AR-V12; S. Sun, et al. Castration resistance inhuman prostate cancer is conferred by a frequently occurring androgenreceptor splice variant. J Clin Invest.(2010) 120(8). 2715-2730).Nonlimiting examples of AR mutations conferring antiandrogen resistanceare: W741L, T877A, and F876L (J. D. Joseph et A clinically relevantandrogen receptor mutation confers resistance to second-generationantiandrogens enzalutamide and ARN-509. Cancer Discov.(2013) 3(9),1020-1029) mutations. Many other LBD resistance conferring mutations areknown in the art and will continue to he discovered. AR-V7 is a splicevariant of AR that lacks the LBD (A. H. Bryce & E. S. Antonarakis.Androgen receptor splice variant 7 in castration-resistant prostatecancer: Clinical considerations. Int J Urol.(2016 Jun 3) 23(8), 646-53.doi: 10.1111/iju.13134). It is constitutively active and has beendemonstrated to he responsible for aggressive PCa and resistance toendocrine therapy.

The invention encompasses novel selective androgen receptor degrader(SARD) compounds of formulas I-IX, IA-ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB which bind to the AR through an alternate binding anddegradation domain (BDD), e.g., the NTD or AF-1. The SARDs may furtherbind the AR ligand binding domain (LBD).

The SARD compounds may be used in treating CRPC that cannot be treatedwith any other antagonist. The SARD compounds may treat CRPC bydegrading AR-SVs. The SARD compounds may maintain their antagonisticactivity in AR mutants that normally convert AR antagonists to agonists.For instance, the SARD compounds maintain their antagonistic activity toAR mutants W741L, T877A, and F876L (J. D. Joseph et al. A clinicallyrelevant androgen receptor mutation confers resistance tosecond-generation antiandrogens enzalutamide and ARN-509. Cancer Discos.(2013) 3(9), 1020-1029). Alternatively, the SARD compounds elicitantagonistic activity within an altered cellular environment in whichLBD-targeted agents are not effective or in which NTD-dependent ARactivity is constitutively active.

Selective Androgen Receptor Degrader (SARD) Compounds

The invention encompasses selective androgen receptor degrader (SARD)compounds represented by the structure of formula I:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

A is R² or R¹;

R² is a five or six-membered saturated or unsaturated ring having atleast one nitrogen atom and 0, 1, or 2 double bonds. optionallysubstituted with at least one of Q¹, Q², Q³, or Q⁴, each independentlyselected from hydrogen, keto, substituted or unsubstituted linear orbranched alkyl, substituted or unsubstituted cycloalkyl, substituted orunsubstituted heterocycloalkyl, haloalkyl, CF₃, substituted orunsubstituted aryl, substituted or unsubstituted phenyl, F, Cl, Br, I,CN, hydroxyl, alkoxy, OR, arylalkyl, NCS, maleimide, NHCOOR, N(R)₂,NHCOR, CONHR, COOR or COR;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate, thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted;

or its optical isomer, or a racemic mixture thereof, isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

In various embodiments, the SARD compound of formula I has a chiralcarbon. In other embodiments, the SARD compound of formula I is aracemic mixture. In other embodiments, the SARD compound of formula I isan (S) isomer. In other embodiments, the SARD compound of formula I isan (R) isomer.

The invention encompasses selective androgen receptor degrader (SARD)compounds represented by the structure of formula IA:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)1;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

A is R² or R³;

R² is a five or six-membered saturated or unsaturated ring having atleast one nitrogen atom and 0, 1, or 2 double bonds, optionallysubstituted with at least one of Q¹. Q², Q³, or Q⁴, each independentlyselected from hydrogen, keto, substituted or unsubstituted linear orbranched alkyl, substituted or unsubstituted cycloalkyl, substituted orunsubstituted heterocycloalkyl, haloalkyl, CF₃, substituted orunsubstituted aryl, substituted or unsubstituted phenyl, F, Cl, Br, I,CN, NO₂, hydroxyl, alkoxy, OR, arylalkyl, NCS, maleimide, NHCOOR, N(R)₂,NHCOR, CONHR, COOR or COR;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate, thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted;

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,polymorph, hydrate or any combination thereof.

The invention encompasses selective androgen receptor degrader (SARD)compounds represented by the structure of formula IB:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

A is R² or R³;

R² is a five or six-membered saturated or unsaturated ring having atleast one nitrogen atom and 0, 1, or 2 double bonds, optionallysubstituted with at least one of Q¹, Q², Q³, or Q⁴, each independentlyselected from hydrogen, keto, substituted or unsubstituted linear orbranched alkyl, substituted or unsubstituted cycloalkyl, substituted orunsubstituted heterocycloalkyl, haloalkyl, CF₃, substituted orunsubstituted aryl, substituted or unsubstituted phenyl, F, Cl, Br, I,CN, NO₂, hydroxyl, alkoxy, OR, arylalkyl, NCS, maleimide, NHCOOR, N(R)₂,NHCOR, CONHR, COOR or COR;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate, thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted;

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,polymorph, hydrate or any combination thereof.

The invention encompasses selective androgen receptor degrader (SARD)compounds represented by the structure of formula IC:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂CH₂Cl,aryl, F, Cl, Br, I, or OH;

R² is a five or six-membered saturated or unsaturated ring having atleast one nitrogen atom and 0, 1, or 2 double bonds. optionallysubstituted with at least one of Q¹, Q², Q³, or Q⁴, each independentlyselected from hydrogen, keto, substituted or unsubstituted linear orbranched alkyl, substituted or unsubstitutai cycloalkyl, substituted orunsubstitutai heterocycloalkyl, haloalkyl, CF₃, substituted orunsubstituted aryl, substituted or unsubstitutai phenyl, F, Cl, Br, I,CN, hydroxyl, alkoxy, OR, arylalkyl, NCS, maleimide, NHCOOR, N(R)₂,NHCOR, CONHR, COOR or COR;

or its optical isomer or a racemic mixture thereof, isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

The invention encompasses selective androgen receptor degrader (SARD)compounds represented by the structure of formula ID:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate. thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ H, is alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted;

or its optical isomer or a racemic mixture thereof, isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof;

wherein if R³ is Br or I, R¹ is CH₃, and T is OH, then X is N or theaniline ring forms a fused heterocyclic ring.

The invention encompasses a SARD compound represented by the structureof formula II:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR.

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

A is R² or ³;

R² is a pyrrole, pyrroline, pyrrolidine, pyrazole, pyrazoline,pyrazolidine, triazole, imidazole, imidazoline, imidazolidine, ormorpholine ring, said ring optionally substituted with at least one ofQ¹, Q², Q³, or Q⁴, each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate. thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted;

or its optical isomer or a reacmic mixture thereof, isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

In various embodiments, the SARD compound of formula II has a chiralcarbon. In other embodiments, the SARD compound of formula II is aracemic mixture. In other embodiments, the SARD compound of formula IIis an (5) isomer. In other embodiments, the SARD compound of formula IIis an (R) isomer.

The invention encompasses a SARD compound represented by the structureof formula IIA:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COON, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

A is R² or R³;

R² is a pyrrole, pyrroline, pyrrolidine, pyrazole, pyrazoline,pyrazolidine, triazole, imidazole, imidazoline, imidazolidine, ormorpholine ring, said ring optionally substituted with at least one ofQ¹, Q², Q², or Q⁴, each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, CI, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR;

R³ is NHR², halide. N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate, thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted;

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,polymorph, hydrate or any combination thereof.

The invention encompasses a SARD compound represented by the structureof formula IIB:

wherein

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

A is R² or R³;

R² a pyrrole, pyrroline, pyrrolidine, pyrazole, pyrazoline,pyrazolidine, triazole, imidazole, imidazoline, imidazolidine, ormorpholine ring, said ring optionally substituted with at least one ofQ¹, Q², Q², or Q⁴, each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, CI, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate, thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted; or its isomer or a racemic mixture thereof,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

The invention encompasses a SARD compound represented by the structureof formula III:

wherein

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COON, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

A is R² or R³;

R² is a pyrrole, pyrroline, pyrrolidine, pyrazole, pyrazoline,pyrazolidine, triazole, imidazole, imidazoline, imidazolidine, ormorpholine ring. said ring optionally substituted with at least one ofQ¹, Q², Q³, or Q⁴, each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N-heterocycle), NO₂, cyanate, isocyanate, thiocyanate,isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ or OPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted;

or its optical isomer or a racemic mixture thereof, isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

In various embodiments, the SARD compound of formula III has a chiralcarbon. In other embodiments, the SARD compound of formula III is aracemic mixture. In other embodiments, the SARD compound of formula IIIis an (S) isomer. In other embodiments, the SARD compound of formula IIIis an (R) isomer.

The invention encompasses a selective androgen receptor degradercompound represented by the structure of formula IV:

wherein

B¹, B², B³, and B⁴ are each independently carbon or nitrogen;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; and

Q¹, Q², Q^(l), or Q⁴ are each independently selected from hydrogen,keto, substituted or unsubstituted linear or branched alkyl, substitutedor unsubstituted cycloalkyl, substituted or unsubstitutedheterocycloalkyl, haloalkyl, CF₃, substituted or unsubstituted aryl,substituted or unsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl,alkoxy, OR, arylalkyl, NCS, maleimide. NHCOOR, N(R)₂, NHCOR, CONHR, COORor COR; wherein if B¹, B², B¹, or B⁴ is nitrogen then Q¹, Q², Q³, or Q⁴,respectively, is nothing; or its optical isomer or a racemic mixturethereof, isomer, pharmaceutically acceptable salt, pharmaceuticalproduct, polymorph, hydrate or any combination thereof.

In various embodiments, the SARD compound of formula IV has a chiralcarbon. In other embodiments, the SARD compound of formula IV is aracemic mixture. In other embodiments, the SARD compound of formula IVis an (S) isomer. In other embodiments, the SARD compound of formula IVis an (R) isomer.

The invention encompasses a selective androgen receptor degradercompound represented by the structure of formula V:

wherein

B¹ and B² are each independently carbon or nitrogen;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; and

Q¹, Q², Q³, or Q⁴ are each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR;wherein if B¹ or B² is nitrogen then Q¹ or Q², respectively, is nothing;or its optical isomer, or a racemic mixture thereof isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

In various embodiments, the SARD compound of formula V has a chiralcarbon. In other embodiments, the SARD compound of formula V is aracemic mixture. In other embodiments, the SARD compound of formula V isan (S) isomer. In other embodiments, the SARD compound of formula V isan (R) isomer.

The invention encompasses a selective androgen receptor degradercompound represented by the structure of formula VI:

wherein

is a single or double bond;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COON, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; and

Q¹, Q², Q³, or Q⁴ are each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide. NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR: orits optical isomer, or a racemic mixture thereof. isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

In various embodiments, the SARD compound of formula VI has a chiralcarbon. In other embodiments, the SARD compound of formula VI is aracemic mixture. In other embodiments, the SARD compound of formula VIis an (S) isomer. In other embodiments, the SARD compound of formula VIis an (R) isomer.

The invention encompasses a selective androgen receptor degradercompound represented by the structure of formula VII:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COON, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂CH₂Cl,aryl, F, Cl, Br, I, or OH; and

Q², Q³, or Q⁴ are each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR: orits optical isomer, or a racemic mixture thereof, isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

In various embodiments, the SARD compound of formula VII has a chiralcarbon. In other embodiments, the SARD compound of formula VII is aracemic mixture. In other embodiments, the SARD compound of formula VIIis an (S) isomer. In other embodiments, the SARD compound of formula VIIis an (R) isomer.

The invention encompasses a selective androgen receptor degradercompound represented by the structure of formula VIIA:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; and

Q², Q³, or Q⁴ are each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR; orits isomer, pharmaceutically acceptable salt, pharmaceutical product,polymorph, hydrate or any combination thereof.

The invention encompasses a selective androgen receptor degradercompound represented by the structure of formula VIIB:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂CH₂Cl,aryl, F, Cl, Br, I, or OH; and

Q², or Q⁴ are each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide. NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR; orits isomer, pharmaceutically acceptable salt, pharmaceutical product,polymorph, hydrate or any combination thereof.

In another embodiment, the invention encompasses a selective androgenreceptor degrader compound represented by the structure of formula VIII:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CF13, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂CH₂Cl,aryl, F, Cl, Br, I, or OH; and

Q², Q³, and Q⁴ are each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR; orits optical isomer, or a racemic mixture thereof isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

In another embodiment, the invention encompasses a selective androgenreceptor degrader compound represented by the structure of formulaVIIIA:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; and

Q³ and Q⁴ are each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR; orits isomer, pharmaceutically acceptable salt, pharmaceutical product,polymorph, hydrate or any combination thereof.

In another embodiment, the invention encompasses a selective androgenreceptor degrader compound represented by the structure of formulaVIIIB:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

and

Q³ and Q⁴ are each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR; or its isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof.

In another embodiment, the invention encompasses a selective androgenreceptor degrader compound represented by the structure of formula IX:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COON, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; and

Q⁴ is selected from hydrogen, keto, substituted or unsubstituted linearor branched alkyl, substituted or unsubstituted cycloalkyl, substitutedor unsubstituted heterocycloalkyl, haloalkyl, is CF₃, substituted orunsubstituted aryl, substituted or unsubstituted phenyl, F, Cl, Br, I,CN, hydroxyl, alkoxy, OR, arylalkyl, NCS, maleimide, NHCOOR, N(R)₂,NHCOR, CONHR, COOR or COR; or its optical isomer, or a racemic mixturethereof, isomer, pharmaceutically acceptable salt, pharmaceuticalproduct, polymorph, hydrate or any combination thereof.

In another embodiment, the invention encompasses a selective androgenreceptor degrader compound represented by the structure of formula IXA:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COON, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; and

Q⁴ is selected from hydrogen, keto, substituted or unsubstituted linearor branched alkyl, substituted or unsubstituted cycloalkyl, substitutedor unsubstituted heterocycloalkyl, haloalkyl, CF₃, substituted orunsubstituted aryl, substituted or unsubstituted phenyl, F, Cl, Br, I,CN, hydroxyl, alkoxy, OR, arylalkyl, NCS, maleimide, NHCOOR, N(R)₂,NHCOR, CONHR, COOR or COR; or its isomer, pharmaceutically acceptablesalt, pharmaceutical product, polymorph, hydrate or any combinationthereof.

In another embodiment, the invention encompasses a selective androgenreceptor degrader compound represented by the structure of formula IXB:

wherein

X is CH or N;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z is H, NO₂, CN, halide, COOH, COR, NHCOR, CONHR,

or Y and Z form a 5 to 8 membered fused ring;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH;

and

Q⁴ is selected from hydrogen, keto, substituted or unsubstituted linearor branched alkyl, substituted or unsubstituted cycloalkyl, substitutedor unsubstituted heterocycloalkyl, haloalkyl, CF₃, substituted orunsubstituted aryl, substituted or unsubstituted phenyl, F, Cl, Br, I,CN, hydroxyl, alkoxy, OR, arylalkyl, NCS, maleimide, NHCOOR, N(R)₂,NHCOR, CONHR, COOR or COR; or its isomer, pharmaceutically acceptablesalt, pharmaceutical product, polymorph, hydrate or any combinationthereof.

In one embodiment, A of formula I-III, IA, IB, IIA, and IIB and R² offormula IC is a five or six-membered saturated or unsaturated ringhaving at least one nitrogen atom. In another embodiment, A is asubstituted or unsubstituted pyrrole, pyrroline, pyrrolidine, pyrazole,pyrazoline, pyrazolidine, imidazole, imidazoline, imidazolidine,triazole, tetrazole, pyridine, morpholine, or other heterocyclic ring.Each represents a separate embodiment of this invention. In anotherembodiment, A is a five or six-membered heterocyclic ring. In anotherembodiment, a nitrogen atom of the five or six membered saturated orunsaturated ring is attached to the backbone structure of the molecule.In another embodiment, a carbon atom of the five or six memberedsaturated or unsaturated ring is attached to the backbone structure ofthe molecule.

In one embodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ offormula ID is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴,OCOR⁴, OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂, CONH(R⁴),CON(R⁴)₂, SR⁴, SO₂R⁴, SOR⁴ SOH, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂,NH(R⁴), N(R⁴)₂, CO(N-heterocycle). NO₂, cyanate, isocyanate,thiocyanate, isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ orOPO(OH)₂; wherein R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl orheteroaryl, wherein said alkyl, haloalkyl, cycloalkyl, aryl orheteroaryl groups are optionally substituted.

In one embodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ offormula ID is NHR². In one embodiment, A of formula I-III, IA, IB, IIA,and IIB and R³ of formula ID is halide, In one embodiment, A of formulaI-III, IA, IB, IIA, and IIB and R³ of formula ID is F. In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R¹ of formulaID is Br. In one embodiment, A of formula I-III, IA, IB, IIA, and IIBand R³ of formula ID is Cl, In one embodiment, A of formula I-III, IA,IB, IIA, and IIB and R³ of formula ID is I. In one embodiment, A offormula I-III, IA, IB, IIA, and IIB and R³ of formula ID is N. In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ of formulaID is OR⁴. In one embodiment, A of formula I-III, IA, IB, IIA, and IIBand R³ of formula ID is CF₃. In one embodiment, A of formula I-III, IA,IB, IIA, and IIB and R³ of formula ID is COR⁴. In one embodiment, A offormula I-III, IA, IB, IIA, and IIB and R³ of formula ID is COCl, In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ of formulaID is COOCOR⁴. In one embodiment, A of formula I-III, IA, IB, IIA, andIIB and R³ of formula ID is COOR⁴. In one embodiment, A of formulaI-III, IA, IB, IIA, and IIB and R³ of formula ID is OCOR⁴. In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ of formulaID is

OCONHR⁴. In one embodiment, A of formula I-III, IA, IB, IIA, and IIB andR³ of formula ID is NHCOOR⁴. In one embodiment, A of formula I-III, IA,IB, IIA, and IIB and R³ of formula ID is NHCONHR⁴. In one embodiment, Aof formula I-III, IA, IB, IIA, and IIB and R³ of formula ID is OCOOR⁴.In one embodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ offormula ID is CN. In one embodiment, A of formula I-III, IA, IB, IIA,and IIB and R³ of formula ID is CON(R⁴)₂. In one embodiment, A offormula I-III, IA, IB, IIA, and IIB and R³ of formula ID is SR⁴. In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ of formulaID is SO₂R⁴. In one embodiment, A of formula I-III, IA, IB, IIA, and IIBand R³ of formula ID is SOR⁴. In one embodiment, A of formula I-III, IA,IB, IIA, and IIB and R³ of formula ID is SO₃H. In one embodiment, A offormula I-III, IA, IB, IIA, and IIB and R³ of formula ID is SO₂NH₂. Inone embodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ offormula ID is SO₂NH(R⁴). In one embodiment, A of formula I-III, IA, IB,IIA, and IIB and R³ of formula ID is SO₂N(R⁴)₂. In one embodiment, A offormula I-III, IA, IB, IIA, and IIB and R³ of formula ID is NH₂. In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ of formulaID is NH(R⁴). In one embodiment, A of formula I-III, IA, IB, IIA, andIIB and R³ of formula ID is N(R⁴)₂. In one embodiment, A of formulaI-III, IA, IB, IIA, and IIB and R³ of formula ID is CONH₂. In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ of formulaID is CONH(R⁴). In one embodiment, A of formula I-III, IA, IB, IIA, andIIB and R³ of formula ID is CO(N-heterocycle). In one embodiment, A offormula I-III, IA, IB, IIA, and IIB and R³ of formula ID is NO₂. In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ of formulaID is cyanate. In one embodiment, A of formula I-III, IA, IB, IIA, andIIB and R³ of formula ID is isocyanate. In one embodiment, A of formulaI-III, IA, IB, IIA, and IIB and R³ of formula ID is thiocyanate. In oneembodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ of formulaID is isothiocyanate. In one embodiment, A of formula I-III, IA, IB,IIA, and IIB and R³ of formula ID is mesylate. In one embodiment, A offormula I-III, IA, IB, IIA, and IIB and R³ of formula ID is tosylate. Inone embodiment, A of formula I-III, IA, IB, IIA, and IIB and R³ offormula ID is triflate. In one embodiment, A of formula I-III, IA, IB,IIA, and IIB and R³ of formula ID is PO(OH)₂. In one embodiment, A offormula I-III, IA, IB, IIA, and IIB and R³ of formula ID is OPO(OH)₂. Inone embodiment, if A is Br or I, R¹ is CH₃, and T is OH, then X is N orthe aniline ring forms a fused heterocyclic ring

In one embodiment R⁴ is H, alkyl, haloalkyl. cycloalkyl, aryl orheteroaryl, wherein said alkyl, haloalkyl, cycloalkyl, aryl orheteroaryl groups are optionally substituted. Each represents a separateembodiment of this invention. In other embodiment, R⁴ is H. In otherembodiments, R⁴ is alkyl. In other embodiments, the alkyl is methyl,ethyl, propyl, isopropyl, butyl, t-butyl, pentyl, neopentyl, iso-pentyl,hexyl, or hepty I, each represents a separate embodiment of thisinvention. In other embodiments, R⁴ is haloalkyl In another embodiment,the haloalkyl is CF₃, CF²CF₃, iodomethyl, bromomethyl, bromoethyl,bromopropyl, each represents a separate embodiment of the invention. Inother embodiments, R⁴ is cycloalkyl. In other embodiments the cycloalkylis cyclobutyl, cyclopentyl, cyclohexyl. In various embodiments, thealkyl, haloalkyl, cycloalkyl, aryl or heteroaryl of R⁴ arc furthersubstituted by one or more groups selected from: halide, CN, CO₂H, OH,SH, NH₂. NO₂, CO₂—(C₁-C₆ alkyl) or O—(C₁-C₆alkyl); each represents aseparate embodiment of this invention.

In a particular embodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ ishydrogen. In a particular embodiment of formulas I-VI, IA-IC, IIA, orIIB, Q¹ is CN. In a particular embodiment of formulas I-VI, IA-IC, IIA,or IIB, Q¹ is F. In a particular embodiment of formulas I-VI, IA-IC,IIA, or IIB, Q¹ is NCS. In a particular embodiment of formulas I-VI,IA-IC, IIA, or IIB, Q¹ is maleimide. In a particular embodiment offormulas I-VI, IA-IC, IIA, or IIB, Q¹ is NHCOOR. In a particularembodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ is N(R):. In aparticular embodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ is CONHR.In a particular embodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ isNHCOR. In a particular embodiment of formulas I-VI, IA-IC, IIA, or IIB,Q¹ is Cl, In a particular embodiment of formulas I-VI, IA-IC, IIA, orIIB, Q¹ is Br. In a particular embodiment of formulas I-VI, IA-IC, IIA,or IIB, Q¹ is I. In a particular embodiment of formulas I-VI, IA-IC,IIA, or IIB, Q¹ is NO₂. In a particular embodiment of formulas I-VI,IA-IC, IIA, or IIB, Q¹ is phenyl. In a particular embodiment of formulasI-VI, IA-IC, IIA, or IIB, Q¹ is 4-fluorophenyl. In a particularembodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ is CF₃. In aparticular embodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ issubstituted or unsubstituted alkyl. In a particular embodiment offormulas I-VI, IA-IC, IIA, or IIB, Q¹ is substituted or unsubstitutedcycloalkyl. In a particular embodiment of formulas I-VI, IA-IC. IIA, orIIB, Q¹ is substituted or unsubstituted heterocycloalkyl. In aparticular embodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ ishaloalkyl. In a particular embodiment of formulas I-VI, IA-IC, IIA, orIIB, Q¹ is substituted or unsubstituted aryl. In a particular embodimentof formulas I-VI, IA-IC, IIA, or IIB, Q¹ is hydroxyl. In a particularembodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ is alkoxy. In aparticular embodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ is OR.

In a particular embodiment of formulas I-VI, IA-IC, IIA, or IIB, Q¹ isarylalkyl. In a particular embodiment of formulas I-VI, IA-IC, IIA, orIIB, Q¹ is amine. In a particular embodiment of formulas I-VI, IA-IC,IIA, or IIB, Q¹ is amide. In a particular embodiment of formulas I-VI.IA-IC, IIA, and IIB, Q¹ is COOR. In a particular embodiment of formulasI-VI, IA-IC, IIA, or IIB, Q¹ is COR. In a particular embodiment offormulas I-VI, IA-IC, IIA, or IIB, Q¹ is keto.

In a particular embodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, orVIIB, Q² is CN. In a particular embodiment of formulas I-VII, IA-IC,IIA, IIB, VIIA, or VIIB, Q² is hydrogen. In a particular embodiment offormulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is keto. In aparticular embodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB,Q² is NCS. In a particular embodiment of formulas I-VII, IA-IC, IIA,IIB, VIIA, or VIIB, Q² is maleimide. In a particular embodiment offormulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is NHCOOR. In aparticular embodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB,Q² is N(R)₂. In a particular embodiment of formulas I-VII, IA-IC, IIA,IIB, VIIA, or VIIB, Q² is CONHR. In a particular embodiment of formulasI-VII, IA-IC, IIA, IIB, VIIA, or VHS, Q² is NHCOR. In a particularembodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is F.In a particular embodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, orVIIB, Q² is Cl, In a particular embodiment of formulas I-VII, IA-IC,IIA, IIB, VIIA, or VIIB, Q² is Br. In a particular embodiment offormulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is I. In a particularembodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is NO₂.In a particular embodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, orVIIB, Q² is phenyl. In a particular embodiment of formulas I-VII, IA-IC,IIA, IIB, VIIA, or VIIB, Q² is 4-fluorophenyl. In a particularembodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is CF₃.In a particular embodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, orVIIB, Q² is substituted or unsubstituted alkyl. In a particularembodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² issubstituted or unsubstituted cycloalkyl. In a particular embodiment offormulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is substituted orunsubstituted heterocycloalkyl. In a particular embodiment of formulas IVII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is haloalkyl. In a particularembodiment of formulas I VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² issubstituted or unsubstituted aryl. In a particular embodiment offormulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is hydroxyl. In aparticular embodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB,Q² is alkoxy. In a particular embodiment of formulas I-VII, IA-IC, IIA,IIB, VIIA, or VIIB, Q² is OR. In a particular embodiment of formulasI-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is arylalkyl. In a particularembodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² isamine. In a particular embodiment of formulas I-VII, IA-IC, IIA, IIB,VIIA, or VIIB, Q² is amide. In a particular embodiment of formulasI-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is COOR. In a particularembodiment of formulas I-VII, IA-IC, IIA, IIB, VIIA, or VIIB, Q² is COR.

In a particular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA,VIIB, VIIIA or VIIIB, Q³ is CN. In a particular embodiment of formulasI-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is F. In aparticular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA. VIIB,VIIIA or VIIIB, Q³ is NCS. In a particular embodiment of formulasI-VIII, IA-IC, IIA. IIB, VIIA, VIIB, VIIIA or VMS, Q³ is maleimide. In aparticular embodiment of formulas I-VIII, IA-IC, IIA, IIB, YHA, VIIB,VIIIA or VIIIB, Q³ is NHCOOR. In a particular embodiment of formulasI-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is N(R)₂. In aparticular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA or VIIIB, Q³ is CONHR. In a particular embodiment of formulasI-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³, is NHCOR. In aparticular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA or VIIIB, Q³ is hydrogen. In a particular embodiment of formulasI-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is keto. In aparticular embodiment of formulas VIII, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA or VIIIB, Q³ is Cl, In a particular embodiment of formulas I-VIII,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is Br. In a particularembodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA orVIIIB, Q³ is I. In a particular embodiment of formulas I-VIII, IA-IC,IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is NO₂. In a particularembodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA orVIIIB, Q³ is phenyl. In a particular embodiment of formulas I-VIII,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is 4-fluorophenyl. In aparticular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA or VIIIB, Q³ is CF₃. In a particular embodiment of formulasI-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is substitutedor unsubstituted alkyl. In a particular embodiment of formulas I-VIII,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is substituted orunsubstituted cycloalkyl. In a particular embodiment of formulas I-VIII,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is substituted orunsubstituted heterocycloalkyl. In a particular embodiment of formulasI-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIB. Q³ is haloalkyl. Ina particular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA or VIIIB, Q³ is substituted or unsubstituted aryl. In a particularembodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA orVIIIB, Q³ is hydroxyl. In a particular embodiment of formulas I-VIII,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is alkoxy. In aparticular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA or VIIIB, Q³ is OR. In a particular embodiment of formulas I-VIII,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is arylalkyl. In aparticular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA or VIIIB, Q³ is amine. In a particular embodiment of formulasI-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is amide. In aparticular embodiment of formulas I-VIII, IA-IC, IIA, IIB, VIIA, VHS,VIIIA or VIIIB, Q³ is COOR. In a particular embodiment of formulasI-VIII, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA or VIIIB, Q³ is COR.

In a particular embodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is CN. In a particular embodiment offormulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴is F. In a particular embodiment of formulas I-IX, IA-IC. IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is NCS. In a particularembodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB,IXA or IXB, Q⁴ is maleimide. In a particular embodiment of formulasI-IX, IA-IC, IIA, IIB, YIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ isNHCOOR. In a particular embodiment of formulas I-IX, IA-IC, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is N(R)₂. In a particularembodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB,IXA or IXB, Q⁴ is CONHR. In a particular embodiment of formulas I IX,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴, is NHCOR. Ina particular embodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA or IXB, Q⁴ is hydrogen. In a particular embodiment offormulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴is keto. In a particular embodiment of formulas I-IX, IA-IC, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB B, Q⁴ is Cl. In a particularembodiment of formulas I-IX. IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB,IXA or IXB, Q⁴ is Br. In a particular embodiment of formulas I-IX,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is I. In aparticular embodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA or IXB, Q⁴ is NO₂. In a particular embodiment offormulas I-IX, IA-IC, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ isphenyl. In a particular embodiment of formulas I-IX, IA-IC, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is 4-fluorophenyl. In aparticular embodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA or IXB, Q⁴ is CF₃. In a particular embodiment offormulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴is substituted or unsubstitutai alkyl. In a particular embodiment offormulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴is substituted or unsubstituted cycloalkyl. In a particular embodimentof formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB,Q⁴ is substituted or unsubstituted heterocycloalkyl. In a particularembodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB,IXA or IXB, Q⁴ is haloalkyl. In a particular embodiment of formulasI-IX, IA-IC, IIA, IIB, VIIA, VHS, VIIIA, VIIIB, IXA or IXB, Q⁴ issubstituted or unsubstituted aryl. In a particular embodiment offormulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴is hydroxyl. In a particular embodiment of formulas I-IX, IA-IC, IIA,IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is alkoxy. In a particularembodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB,IXA or IXB, Q⁴ is OR. In a particular embodiment of formulas I-IX,IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is arylalkyl.In a particular embodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is amine. In a particular embodimentof formulas I-IX, IA-IC, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB,Q³ is amide. In a particular embodiment of formulas I IX, IA-IC, IIA,IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, Q⁴ is COOR. In a particularembodiment of formulas I-IX, IA-IC, IIA, IIB, VIIA, VHS, VIIIA, VIIIB,IXA or IXB, Q⁴ is COR.

In a particular embodiment of formulas I, IA, IB, IC, ID, II, IIA, IIB,VII, VIIA, VIIB, VIII, VIIIA, VIIIB, IX, IXA or IXB, X is CH. In aparticular embodiment of formulas I, IA, IB, IC, ID, II, IIA, IIB, VII,VIIA, VIIB, VIII, VIIIA, VIIIB, IX, IXA or IXB, X is N.

In some embodiments, wherein if A or R³ is Br or I, R¹ is CH₃, and T isOH, then X is N or the aniline ring forms a fused heterocyclic ring.

In a particular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Y is H. In a particularembodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA, or IXB, Y is CF₃. In a particular embodiment offormulas I IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA,or IXB, Y is F. In a particular embodiment of formulas I-IX, IA, IB, IC,ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Y is I. In aparticular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA, or IXB, Y is Br. In a particular embodiment offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA,or IXB. Y is Cl, In a particular embodiment of formulas I IX, IA, IB,IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Y is CN. In aparticular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA, or IXB, Y is C(R)₃.

In a particular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Z is H. In a particularembodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA, or IXB, Z is NO₂. In a particular embodiment offormulas I-IX. IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA,or IXB, Z is CN. In a particular embodiment of formulas I-IX, IA, IB,IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Z is a halide.In a particular embodiment of formulas I-VII, IA, IB, IC, ID, IIA, IIB,VIIA, or VIIB, Z is F. In a particular embodiment of formulas I-IX, IA,IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Z is Cl, Ina particular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Z is Br. In a particularembodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA, or IXB, Z is I. In a particular embodiment offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA,or IXB, Z is COOH. In a particular embodiment of formulas I-IX, IA, IB,IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Z is COR. In aparticular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA, or IXB, Z is NHCOR. In a particular embodimentof formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB,IXA, or IXB, Z is CONHR.

In a particular embodiment of formulas I I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA, or IXB, Y and Z forms a fused ring withthe phenyl. In other embodiments, the fused ring with the phenyl is a 5to 8 membered ring. In other embodiments, the fused ring with the phenylis a 5 or 6 membered ring. In other embodiments, the ring is acarbocyclic or heterocyclic. In other embodiments. Y and Z form togetherwith the phenyl to form a naphthyl, quinolinyl, benzimidazolyl,indazolyl, indolyl, isoindolyl, indenyl, or quinazolinyl. In aparticular embodiment, Y and Z form together with the phenyl to form aquinazolin-6-yl ring system.

In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII, IXIA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB R¹ is H.In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII, IXIA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, R¹ isCH₃. In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII,IX IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, R¹ isCH₂F. In a particular embodiment of formulas TI, IV, V, VI, VII, VIII,IX IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, R¹ isCHF₂. In a particular embodiment of formulas I, II, IV, V, VI, VII,VIII, IX IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB,R¹ is CF₃. In a particular embodiment of formulas I, II, IV, V, VI, VII,VIII, IX IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB,R¹ is CH₂CH₃. In a particular embodiment of formulas I, II, IV, V, VI,VII, VIII, IX IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA orIXB, R¹ is CF₂CF₃.

In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII, IX,IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, T is H.In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII, IX,IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, T is OH.In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII, IX,IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, T is OR.In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII, IX,IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB. T isOCOR In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII,IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, T isCH₃. In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII,IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, T is—NHCOCH₃. In a particular embodiment of formulas I, II, IV, V, VI, VII,VIII, IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA orIXB, T is NHCOR.

In a particular embodiment of formulas I, II, IV, V, VI, VII, VIII, IX,IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, T and R¹form a 3-8 carbocyclic or heterocyclic ring. In other embodiments. T andR¹ form a 3, 4, 5, 6, 7, or 8 membered carbocyclic or heterocyclic ring.Each represents a separate embodiment of this invention. In someembodiments T and R¹ form a carbocyclic ring such as cyclopropyl,cyclobutyl, cyclopentyl, cyclohexyl, etc. In some embodiments T and R¹form a heterocyclic ring such as piperidine, pyridine, furan, thiophene,pyrrole, pyrazole, pyrimidine, etc.

In a particular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, R is H. In a particular embodimentof formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB,IXA, R is alkyl. In a particular embodiment of formulas I-IX, IA, IB,IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA, R is alkenyl. In aparticular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA, R is haloalkyl. In a particular embodiment offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA,R is alcohol. In a particular embodiment of formulas I-VII, IA, IB, IC,ID, IIA, IIB, VIIA, or VIIB, R is CH₂CH₂OH. In a particular embodimentof formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB,IXA, R is CF₃. In a particular embodiment of formulas I-VII, IA, IB, IC,ID, IIA, IIB, VIIA, or VIIB, R is CH₂Cl, In a particular embodiment offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA,R is CH₂CH₂Cl, In a particular embodiment of formulas I-IX, IA, IB, IC,ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA, R is aryl. In a particularembodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA, R is F, In a particular embodiment of formulas I-IX,IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA, R is Cl, In aparticular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIIIA, VMS, IXA, R is Br. In a particular embodiment of formulasI-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VMS, IXA, R is I. Ina particular embodiment of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA, R is OH.

In a particular embodiment of formula IV, Q¹ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula V, Q¹ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VI, Q¹ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula IV, Q² is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula V, Q² is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VI, Q² is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VII, Q² is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)_(3.)

In a particular embodiment of formula VIIA, Q² is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VIIB, Q² is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula IV, Q³ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula V, Q³ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VI, Q³ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VII, Q¹ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VIII, Q³ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula IV, Q⁴ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula V, Q⁴ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VI, Q⁴ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VII, Q⁴ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VIIA, Q⁴ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VIIB, Q⁴ is H, CN, CF₃, phenyl,4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe or NHCOOC(CH₃)₃.

In a particular embodiment of formula VIII, VIIIA, or VIIIB, Q⁴ is H,CN, CF₃, phenyl, 4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe orNHCOOC(CH₃)₃.

In a particular embodiment of formula IX, IXA, or IXB, Q⁴ is H, CN, CF₃,phenyl, 4-fluorophenyl, F, Br, Cl, I, COMe, NHCOOMe, NHCOMe orNHCOOC(CH₃)₃.

The invention encompasses a selective androgen receptor degrader (SARD)compound selected from any one of the following structures:

As used herein. the term “heterocycle” or “heterocyclic ring” grouprefers to a ring structure comprising in addition to carbon atoms, atleast one atom of sulfur. oxygen, nitrogen or any combination thereof,as part of the ring. The heterocycle may be a 3-12 membered ring; 4-8membered ring; a 5-7 membered ring; or a 6 membered ring. Preferably,the heterocycle is a 5 to 6 membered ring. Typical examples ofheterocycles include, but are not limited to, piperidine, pyridine,furan, thiophene, pyrrole, pyrrolidine, pyrazole, pyrazine, piperazineor pyrimidine. Examples of C₅-C₈ heterocyclic rings include pyran,dihydropyran, tetrahydropyran, dihydropyrrole, tetrahydropyrrole,pyrazine, dihydropyrazine, tetrahydropyrazine, pyrimidine,dihydropyrimidine, to tetrahydropyrimidone, pyrazole, dihydropyrazole,tetrahydropyrazole, triazole, tetrazole, piperazine, pyridine,dihydropyridine, tetrahydropyridine, morpholine, thiomorpholine, furan,dihydrofuran, tetrahydrofuran, thiophene, dihydrothiophene,tetrahydrothiophene, thiazole, imidazole, isoxazole, and the like. Theheterocycle ring may be fused to another saturated or unsaturatedcycloalkyl or a saturated or unsaturated heterocyclic ring. When theheterocycle ring is substituted, the substituents include at least oneof halogen, haloalkyl, hydroxyl, alkoxy, carbonyl, amido, alkylamido,dialkylamido, cyano, nitro, CO₂H, amino, alkylamino, dialkylamino,carboxyl, thiol, or thioalkyl.

The term “aniline ring system” refers to the conserved ring representedto the left of the structures in this document which is substituted byX, Y, and/or Z.

The term “cycloalkyl” refers to a non-aromatic, monocyclic or polycyclicring comprising carbon and hydrogen atoms. A cycloalkyl group can haveone or more carbon-carbon double bonds in the ring so long as the ringis not rendered aromatic by their presence. Examples of cycloalkylgroups include, but are not limited to, (C₃-C₇) cycloalkyl groups, suchas cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl,and saturated cyclic and bicyclic terpenes and (C₃-C₇) cycloalkenylgroups, such as cyclopropenyl, cyclobutenyl, cyclopentenyl,cyclohexenyl, and cycloheptenyl, and unsaturated cyclic and bicyclicterpenes. Examples of C₅-C₈ carbocyclic include cyclopentane,cyclopentane, cyclohexane, and cyclohexane rings. A cycloalkyl group canbe unsubstituted or substituted by at least one substituent. Preferably,the cycloalkyl group is a monocyclic ring or bicyclic ring.

The term “alkyl” refers to a saturated aliphatic hydrocarbon, includingstraight-chained and branched-chained. Typically, the alkyl group has1-12 carbons, 1-7 carbons, 1-6 carbons, or 1-4 carbon atoms. A branchedalkyl is an alkyl substituted by alkyl side chains of 1 to 5 carbons.The branched alkyl may have an alkyl substituted by a C₁-0₅ haloalkyl.Additionally, the alkyl group may be substituted by at least one ofhalogen, haloalkyl, hydroxyl, alkoxy carbonyl, amido, alkylamido,dialkylamido, nitro, CN, amino, alkylamino, dialkylamino, carboxyl, thioor thioalkyl.

An “arylalkyl” group refers to an alkyl bound to an aryl, wherein alkyland aryl are as defined herein. An example of an arylalkyl group is abenzyl group.

An “alkenyl” group refers to an unsaturated hydrocarbon, includingstraight chain and branched chain having one or more double bonds. Thealkenyl group may have 2-12 carbons. preferably the alkenyl group has2-6 carbons or 2-4 carbons. Examples of alkenyl groups include, but arenot limited to, ethenyl, propenyl, butenyl, cyclohexenyl, etc. Thealkenyl group may be substituted by at least one halogen, hydroxy,alkoxy carbonyl, amide, alkylamido, dialkylamido, nitro, amino,alkylamino, dialkylamino, carboxyl, thio, or thioalkyl.

As used herein ther term “aryl” group refers to an aromatic group havingat least one carbocyclic aromatic group or heterocyclic aromatic group,which may be unsubstituted or substituted. When present, substituentsinclude, but are not limited to, at least one halogen, haloalkyl,hydroxy, alkoxy carbonyl, amino, alkylamino, dialkylamido, nitro, amino,alkylamino, dialkylamino, carboxy or thio or thioalkyl. Nonlimitingexamples of aryl rings are phenyl, naphthyl, pyranyl, pyrrolyl,pyrazinyl, pyrimidinyl, pyrazolyl, pyridinyl, (uranyl, thiophenyl,thiazolyl, imidazolyl, isoxazolyl, and the like. The aryl group may be a4-12 membered ring, preferably the aryl group is a 4-8 membered ring.Also the aryl group may be a 6 or 5 membered ring.

The term “heteroaryl” refers to an aromatic group having at least oneheterocyclic aromatic ring. In one embodiment, the heteroaryl comprisesat least one heteroatom such as sulfur, oxygen, nitrogen, silicon,phosphorous or any combination thereof, as part of the ring. In anotherembodiment, the heteroaryl may be unsubstituted or substituted by one ormore groups selected from halogen, aryl, heteroaryl, cyano, haloalkyl,hydroxy, alkoxy carbonyl, amino, alkylamido, dialkylamido, nitro, amino,alkylamino, dialkylamino, carboxy or thio or thioalkyl. Nonlimitingexamples of heteroaryl rings are pyranyl, pyrrolyl, pyrazinyl,pyrimidinyl, pyrazolyl, pyridinyl, furanyl, thiophenyl, thiazolyl,indolyl, imidazolyl, isoxazolyl, and the like. In one embodiment, theheteroaryl group is a 5-12 membered ring. In one embodiment, theheteroaryl group is a five membered ring. In one embodiment, theheteroaryl group is a six membered ring. In another embodiment, theheteroaryl group is a 5-8 membered ring. In another embodiment, theheteroaryl group comprises of 1-4 fused rings. In one embodiment, theheteroaryl group is 1, 2, 3-triazole. In one embodiment the heteroarylis a pyridyl. In one embodiment the heteroaryl is a bipyridyl. In oneembodiment the heteroaryl is a terpyridyl.

As used herein, the term “haloalkyl” group refers to an alkyl group thatis substituted by one or more halogen atoms, e.g. by F, Cl, Br or I.

A “hydroxyl” group refers to an OH group. It is understood by a personskilled in the art that when T, Q¹, Q², Q³, or Q⁴, in the compounds ofthe present invention is OR, then R is not OH.

The term “halogen” or “halo” or “halide” refers to a halogen; F, Cl, Bror I.

In one embodiment, this invention provides the compounds and/or its useand/or, its derivative, optical isomer, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, prodrug, polymorph, crystal or combinations thereof.

In one embodiment, the methods of this invention make use of“pharmaceutically acceptable salts” of the compounds, which may beproduced, by reaction of a compound of this invention with an acid orbase.

The compounds of the invention may be converted into pharmaceuticallyacceptable salts. A pharmaceutically acceptable salt may be produced byreaction of a compound with an acid or base.

Suitable pharmaceutically acceptable salts of amines may be preparedfrom an inorganic acid or from an organic acid. Examples of inorganicsalts of amines include, but are not limited to, bisulfates, borates,bromides, chlorides, hemisulfates, hydrobromates, hydrochlorates,2-hydroxyethylsulfonates (hydroxyethanesulfonates), iodates, iodides,isothionates, nitrates, persulfates, phosphates, sulfates, sulfamates,sulfanilates, sulfonic acids (alkylsulfonates, arylsulfonates, halogensubstituted alkylsulfonates, halogen substituted arylsulfonates),sulfonates, or thiocyanates.

Examples of organic salts of amines may be selected from aliphatic,cycloaliphatic, aromatic, araliphatic, heterocyclic, carboxylic andsulfonic classes of organic acids, examples of which are acetates,arginines, aspartates, ascorbates, adipates, anthranilates, algenates,alkane carboxylases, substituted alkane carboxylates, alginates,benzenesulfonates, benzoates, bisulfates, butyrates, bicarbonates,bitartrates, carboxylases, citrates, camphorates, camphorsulfonates,cyclohexylsul famates, cyclopentanepropionates, calcium edetates,camsylates, carbonates, clavulanates, cinnamates, dicarboxylates,digluconates, dociecylsulfonates, dihydrochlorides, decannates,enanthuates, ethanesulfonates, edetates, edisylates, estolates,esylates, fumarases, formates, fluorides, galacturonates, gluconates,glutamates, glycolates, glucorates, glucoheptanoates, glycerophosphates,gluceptates, glycollylarsanilates, glutarates, glutamates, heptanoates,hexanoates, hydroxymaleates, hydroxycarboxlic acids, hexylresorcinates,hydroxybenzoates, hydroxynaphthoates, hydrofluorates, lactates,lactobionates, laurates, malates, maleates,methylenebis(beta-oxynaphthoate), malonates, mandelates, mesylates,methane sulfonates, methylbromides, methyInitrates, methylsulfonates,monopotassium maleates, mutates, monocarboxylates, nitrates,naphthalenesulfonates, 2-naphthalenesulfonates, nicotinates, napsylates.N-methylglucamines, oxalates, octanoates, oleates, pamoates,phenylacetates, picrates, phenylbenzoates, pivalates, propionates,phthalates, pectinases, phenylpropionates, palmitates, pantothenates,polygalacturates, pyruvates, quinates, salicylates, succinates,stearates, sulfanilates, subacetates, tartarates, theophyllineacetates,p-toluenesulfonates (tosylates), trifluoroacetates, terephthalates,tannates, teoclates, trihaloacetates, triethiodide, tricarboxylates,unciecanoates and valerates. Examples of inorganic salts of carboxylicacids or phenols may be selected from ammonium, alkali metals, andalkaline earth metals. Alkali metals include, but are not limited to,lithium, sodium, potassium, or cesium. Alkaline earth metals include,but are not limited to, calcium, magnesium, aluminium; zinc, barium,cholines, or quaternary ammoniums. Examples of organic salts ofcarboxylic acids or phenols may be selected from arginine, organicamines to include aliphatic organic amines, alicyclic organic amines,aromatic organic amines, benzathines, t-butylamines, benethamines(N-benzylphenethylamine), dicyclohexylamines, ciimethylamines,diethanolamines, ethanolamines, ethylenediamines, hydrabamines,imidazoles, lysines, methylamines, meglamines. N-methyl-D-glucamines.N,N′-ciihenzylethylenediarnines, nicotinamides, organic amines,ornithines, pyridines, picolines, piperazines, procaine,tris(hydroxymethypmethylamines, triethylamines, triethanolamines,trimethylamines, tromethamines and ureas.

In various embodiments, the pharmaceutically acceptable salts of thecompounds of this invention include: HCl salt, oxalic acid salt,L-(+)-tartaric acid salt, HBr salt and succinic acid salt. Eachrepresents a separate embodiment of this invention.

Salts may be formed by conventional means, such as by reacting the freebase or free acid form of the product with one or more equivalents ofthe appropriate acid or base in a solvent or medium in which the salt isinsoluble or in a solvent such as water, which is removed in vacuo or byfreeze drying or by exchanging the ions of a existing salt for anotherion or suitable ion-exchange resin.

The methods of the invention may use an uncharged compound or apharmaceutically acceptable salt of the compound. In particular, themethods use pharmaceutically acceptable salts of compounds of formulasI-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB.The pharmaceutically acceptable salt may be an amine salt ora salt of aphenol of the compounds of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIDA, VIIIB, IXA or IXB.

In one embodiment, the methods of this invention make use of a freebase, free acid, non charged or non-complexed compounds of formulasI-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB,and/or its isomer, pharmaceutical product, hydrate, polymorph, orcombinations thereof.

In one embodiment, the methods of this invention make use of an opticalisomer of a compound of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIDA, VIIIB, IXA or IXB. In one embodiment, the methods of thisinvention make use of an isomer of a compound of formulas I-IX, IA, IB,IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB. In oneembodiment, the methods of this invention make use of a pharmaceuticalproduct of a compound of formulas I-IX. IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA or IXB. In one embodiment, the methods of thisinvention make use of a hydrate of a compound of I-IX, IA, IB, IC, ID,IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB. In one embodiment, themethods of this invention make use of a polymorph of a compound offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXAor IXB. In one embodiment, the methods of this invention make use of ametabolite of a compound of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIDA, VIIIB, IXA or IXB. In another embodiment, the methodsof this invention make use of a composition comprising a compound offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIDA, VIIIB, IXA orIXB, as described herein, or, in another embodiment, a combination ofisomer. metabolite. pharmaceutical product, hydrate, polymorph of acompound of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB.

As used herein, the term “isomer” includes, but is not limited to,optical isomers, structural isomers, or conformational isomers.

The term “isomer” is meant to encompass optical isomers of the SARDcompound. It will be appreciated by those skilled in the art that theSARDs of the present invention contain at least one chiral center.Accordingly, the compounds may exist as optically-active (such as an (R)isomer or (S) isomer) or racemic forms. Optically active compounds mayexist as enantiomerically enriched mixtures. Some compounds may alsoexhibit polymorphism. It is to he understood that the present inventionencompasses any racemic, optically active, polymorphic, orstereroisomeric form, or mixtures thereof. Thus, the invention mayencompass SARD compounds as pure (R)-isomers or as pure (5)-isomers. Itis known in the art how to prepare optically active forms. For example,by resolution of the racemic form by recrystallization techniques, bysynthesis from optically active starting materials, by chiral synthesis,or by chromatographic separation using a chiral stationary phase.

Compounds of the invention may be hydrates of the compounds. As usedherein, the term “hydrate” includes, but is not limited to, hemihydrate,monohydrate, dihydrate, or trihydrate. The invention also includes useof N-oxides of the amino substituents of the compounds described herein.

This invention provides, in other embodiments, use of metabolites of thecompounds as herein described. In one embodiment. “metabolite” means anysubstance produced from another substance by metabolism or a metabolicprocess.

In one embodiment, the compounds of this invention are preparedaccording to Example 1.

Biological Activity of Selective Androgen Receptor Degraders

A method of treating prostate cancer (PCa) or increasing the survival ofa male subject suffering from prostate cancer comprising administeringto the subject a therapeutically effective amount of a compound or itspharmaceutically acceptable salt, represented by a compound of formulaI:

wherein

T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR;

R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;

or T and R¹ form a 3-8 carbocyclic or heterocyclic ring;

Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃;

Z H, is NO₂, CN, halide, COOH, COR, NHCOR, CONHR, or Y and Z form a 5 to8 membered ring;

X is CH or N;

R is H, alkyl, alkenyl, haloalkyl, alcohol, CH₂CH₂OH, CF₃, CH₂Cl,CH₂CH₂Cl, aryl, F, CI, Br, I, or OH;

A is R² or R¹;

R² is a five-membered saturated or unsaturated ring having at least onenitrogen atom and 0, 1, or 2 double bonds, optionally substituted withat least one of Q¹, Q², Q³, or Q⁴, each independently selected fromhydrogen, keto, substituted or unsubstituted linear or branched alkyl,substituted or unsubstituted cycloalkyl, substituted or unsubstitutedheterocycloalkyl, haloalkyl, CF₃, substituted or unsubstituted aryl,substituted or unsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl,alkoxy, OR, benzyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR orCOR;

R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴,OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH2, CONH(R4), CON(R4)2, SR⁴,SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂,CO(N- heterocycle), C(O)(C₁-C₁₀)alkyl, NO₂, cyanate, isocyanate,thiocyanate, isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂orOPO(OH)₂; and

R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl, wherein saidalkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups are optionallysubstituted; or its optical isomer, or a racemic mixture thereof,isomer, pharmaceutically acceptable salt, pharmaceutical product,polymorph, hydrate or any combination thereof.

A method of treating prostate cancer (PCa) or increasing the survival ofa male subject suffering from prostate cancer comprising administeringto the subject a therapeutically effective amount of a compound or itspharmaceutically acceptable salt, or isomer, represented by a compoundof formulas I-IX, IA-ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB.

The prostate cancer may be advanced prostate cancer, refractory prostatecancer, castration resistant prostate cancer (CRPC), metastatic CRPC(mCRPC), non-metastatic CRPC (nmCRPC), high-risk nmCRPC or anycombination thereof.

The prostate cancer may depend on AR-FL and/or AR-SV for proliferation.The prostate or other cancer may be resistant to treatment with anandrogen receptor antagonist. The prostate or other cancer may beresistant to treatment with enzalutamide, bicalutamide, abiraterone,ARN-509, ODM-201, EPI-001, EPI-506, AZD-3514. galeterone. ASC-79,flutamide, hydroxyflutamide, nilutamide, cyproterone acetate,ketoconazole, spironolactone, or any combination thereof. The method mayalso reduce the levels of AR, AR-FL, AR-FL with antiandrogenresistance-conferring AR-LBD mutations, AR-SV, gene-amplified AR, or anycombination thereof.

In one embodiment, this invention provides a method of treatingenzalutamide resistant prostate cancer comprising administering to thesubject a therapeutically effective amount of a compound of thisinvention, or its optical isomer, isomer, pharmaceutically acceptablesalt, pharmaceutical product, polymorph, hydrate or any combinationthereof.

In one embodiment, this invention provides a method of treatingabiraterone resistant prostate cancer comprising administering to thesubject a therapeutically effective amount of a compound of thisinvention, or its optical isomer, isomer, pharmaceutically acceptablesalt, pharmaceutical product, polymorph, hydrate or any combinationthereof.

In one embodiment, this invention provides a method of treating triplenegative breast cancer (TIBC) comprising administering to the subject atherapeutically effective amount of a compound of this invention, or itsoptical isomer, isomer, pharmaceutically acceptable salt, pharmaceuticalproduct, polymorph, hydrate or any combination thereof.

The method may further comprise a second therapy such as androgendeprivation therapy (ADT) or LHRH agonist or antagonist. LHRH agonistsinclude, but are not limited to, leuprolide acetate.

The invention encompasses a method of treating or inhibiting theprogression of prostate cancer (PCa) or increasing the survival of amale subject suffering from prostate cancer comprising administering tothe subject a therapeutically effective amount of a SARD compound orpharmaceutically acceptable salt, wherein the compound is at least oneof compounds 1001 to 1064 and 1069 to 1071.

The invention encompasses a method of treating or inhibiting theprogression of refractory prostate cancer (PCa) or increasing thesurvival of a male subject suffering from refractory prostate cancercomprising administering to the subject a therapeutically effectiveamount of a SARD compound or pharmaceutically acceptable salt, whereinthe compound is represented by a compound of formulas I-IX, IA, IB, IC,ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or the compound isat least one of compounds 1001 to 1064 and 1069 to 1071.

The invention encompasses a method of treating or increasing thesurvival of a male subject suffering from castration resistant prostatecancer (CRPC) comprising administering to the subject a therapeuticallyeffective amount of a SARD wherein the compound is represented by acompound of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB, or at least one of compounds 1001 10 1064 and 1069 to1071.

The method may further comprise administering androgen deprivationtherapy to the subject.

The invention encompasses a method of treating or inhibiting theprogression of enzalutamide resistant prostate cancer (PCa) orincreasing the survival of a male subject suffering from enzalutamideresistant prostate cancer comprising administering to the subject atherapeutically of amount of a SARD compound or pharmaceuticallyacceptable salt, wherein the compound is represented by a compound offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXAor IXB, or the compound is at least one of compounds 1001 to 1064 and1069 to 1071.

The method may further comprise administering androgen deprivationtherapy to the subject.

The invention encompasses a method of treating or inhibiting theprogression of triple negative breast cancer (TNBC) or increasing thesurvival of a female subject suffering from triple negative breastcancer comprising administering to the subject a therapeuticallyeffective amount of a SARD compound or pharmaceutically acceptable salt,wherein the compound is represented by a compound of formulas I-IX, IA,IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or thecompound is at least one of compounds 1001 to 1064 and 1069 to 1071.

The invention encompasses a method of treating breast cancer in asubject in need thereof, wherein said subject has AR expressing breastcancer. AR-SV expressing breast cancer, and/or AR-V7 expressing breastcancer. comprising administering to the subject a therapeuticallyeffective amount of a selective androgen receptor degrader (SARD)compound, or its isomer, pharmaceutically acceptable salt,pharmaceutical product, polymorph, hydrate or any combination thereof.wherein said SARD compound is represented by the structure of formulaI-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, orthe compound is at least one of compounds 1001 to 1064 and 1069 to 1071.

The invention encompasses a method of treating AR expressing breastcancer in a subject in need thereof, comprising administering to thesubject a therapeutically effective amount of a selective androgenreceptor degrader (SARD) compound, or its isomer, pharmaceuticallyacceptable salt, pharmaceutical product, polymorph, hydrate or anycombination thereof. wherein said SARD compound is represented by thestructure of formula I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB, or the compound is at least one of compounds 1001 to1064 and 1069 to 1071.

The invention encompasses a method of treating AR-SV expressing breastcancer in a subject in need thereof, comprising administering to thesubject a therapeutically effective amount of a selective androgenreceptor degrader (SARD) compound, or its isomer, pharmaceuticallyacceptable salt, pharmaceutical product, polymorph, hydrate or anycombination thereof, wherein said SARD compound is represented by thestructure of formula I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB, or the compound is at least one of compounds 1001 (01064 and 1069 to 1071.

The invention encompasses a method of treating AR-V7 expressing breastcancer in a subject in need thereof, comprising administering to thesubject a therapeutically effective amount of a selective androgenreceptor degrader (SARD) compound, or its isomer, pharmaceuticallyacceptable salt, pharmaceutical product, polymorph, hydrate or anycombination thereof, wherein said SARD compound is represented by thestructure of formula I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB, or the compound is at least one of compounds 1001 to1064 and 1069 to 1071.

As used herein, the term “increase the survival” refers to a lengtheningof time when describing the survival of a subject. Thus in this context,the compounds of the invention may be used to increase the survival ofmen with advanced prostate cancer. refractory prostate cancer,castration resistant prostate cancer (CRPC); metastatic CRPC (mCRPC);non-metastatic CRPC (nmCRPC); or high-risk nmCRPC; or women with TNBC.

Alternatively, as used herein. the terms “increase”, increasing“, or“increased” may be used interchangeably and refer to an entity becomingprogressively greater (as in size, amount, number, or intensity),wherein for example the entity is sex hormone-binding globulin (SIIBG)or prostate-specific antigen (PSA).

The compounds and compositions of the invention may be used forincreasing metastasis-free survival (MFS) in a subject suffering fromnon-metastatic prostate cancer. The non-metastatic prostate cancer maybe non-metastatic advanced prostate cancer. non-metastatic CRPC(nmCRPC), or high-risk nmCRPC.

The SARD compounds described herein may be used to provide a dualaction. For example, the SARD compounds may treat prostate cancer andprevent metastasis. The prostate cancer may be refractory prostatecancer; advanced prostate cancer; castration resistant prostate cancer(CRPC); metastatic CRPC (mCRPC); non-metastatic CRPC (nmCRPC); orhigh-risk nmCRPC.

The SARD compounds described herein may be used to provide a dualaction. For example, the SARD compounds may treat TNBC and preventmetastasis.

Men with advanced prostate cancer who are at high risk for progressionto castration resistant prostate cancer (CRPC) are men on ADT with serumtotal testosterone concentrations greater than 20 ng/dL or men withadvanced prostate cancer who at the time of starting ADT had either (1)confirmed Gleason pattern 4 or 5 prostate cancer, (2) metastaticprostate cancer, (3) a PSA doubling time <3 months, (4) a PSA ≥20 ng/mL,or (5) a PSA relapse in <3 years after definitive local therapy (radicalprostatectomy or radiation therapy).

Normal levels of prostate specific antigen (PSA) are dependent onseveral factors, such as age and the size of a male subject's prostate,among others. PSA levels in the range between 2.5-10 ng/mL areconsidered “borderline high” while levels above 10 ng/mL are considered“high.” A rate change or “PSA velocity” greater than 0.75/year isconsidered high. PSA levels may increase despite ongoing ADT or ahistory of ADT, surgical castration or despite treatment withantiandrogens and/or LHRH agonist.

Men with high risk non-metastatic castration resistant prostate cancer(high-risk nmCRPC) may include those with rapid PSA doubling times,having an expected progression-free survival of approximately 18 monthsor less (Miller K. Moul J W, Gleave M. et al. 2013. “Phase III,randomized, placebo-controlled study of once-daily oral zibotentan(ZD4054) in patients with non-metastatic castration-resistant prostatecancer.” Prostate Canc Prost Dis. February; 16:187-192). This relativelyrapid progression of their disease underscores the importance of noveltherapies for these individuals.

The methods of the invention may treat subjects with PSA levels greaterthan 8 ng/mL where the subject suffers from high-risk nmCRPC. Thepatient population includes subjects suffering from nmCRPC where PSAdoubles in less than 8 months or less than 10 months. The method mayalso treat patient populations where the total serum testosterone levelsare greater than 20 ng/mL in a subject suffering from high-risk nmCRPC.In one case. the serum free testosterone levels are greater than thoseobserved in an orchiectomized male in a subject suffering from high-risknmCRPC.

The pharmaceutical compositions of the invention may further comprise atleast one LHRH agonist or antagonist, antiandrogen, anti-programmeddeath receptor 1 (anti-PD-1) drug or anti-PD-L1 drug. LHRH agonistsinclude, but are not limited to, leuprolide acetate (Luprone) (U.S. Pat.Nos. 5,480,656; 5,575,987; 5,631,020; 5,643,607; 5,716,640; 5,814,342;6,036,976 hereby incorporated by reference) or goserelin acetate(Zoladex®) (U.S. Pat. Nos. 7,118,552; 7,220,247; 7,500,964 herebyincorporated by reference). LHRH antagonists include, but are notlimited to, degarelix or abarelix. Antiandrogens include, but are notlimited to, bicalutamide, flutamide, apalutamide, finasteride,dutasteride, enzalutamide, nilutamide, chlormadinone, abiraterone, orany combination thereof. Anti-PD-1 drugs include, but are not limitedto, AMP-224, nivolumab, pembrolizumab, pidilizumab, and AMP-554.Anti-PD-L1 drugs include, but are not limited to, BMS-936559.atezolizumab, durvalumab, avelumab, and MPDL3280A. Anti-CTLA-4 drugsinclude, but are not limited to, ipilimumab and tremelimumab.

Treatment of prostate cancer, advanced prostate cancer, CRPC, mCRPCand/or nmCRPC may result in clinically meaningful improvement inprostate cancer related symptoms, function and/or survival. Clinicallymeaningful improvement can be determined by an increase in radiographicprogression free survival (rPFS) if cancer is metastatic, or an increasemetastasis-free survival (MFS) if cancer is non-metastatic, amongothers.

The invention encompasses methods of lowering serum prostate specificantigen (PSA) levels in a male subject suffering from prostate cancer,advanced prostate cancer, metastatic prostate cancer or castrationresistant prostate cancer (CRPC) comprising administering atherapeutically effective amount of a SARD compound, wherein thecompound is represented by the structure of formulas I-IX, IA, IB, IC,ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or the compound is atleast one of compounds 1001 to 1064 and 1069 to 1071.

The invention encompasses a method of secondary hormonal therapy thatreduces serum PSA in a male subject suffering from castration resistantprostate cancer (CRPC) comprising administering a therapeuticallyeffective amount of a compound of formulas I-IX, IA, IB, IC, ID, IIA,IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or the compound is at leastone of compounds 1001 to 1064 and 1069 to 1071 that reduces serum PSA ina male subject suffering from castration resistant prostate cancer.

The invention encompasses a method of reducing levels of A.R. AR-fulllength (AR-FL). AR-FL with antiandrogen resistance-conferring AR-LBDmutations, AR-splice variant (AR-SV), and/or amplifications of the ARgene within the tumor in the subject in need thereof comprisingadministering a therapeutically effective amount of a compound offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXAor IXB or the compound is at least one of compounds 1001 to 1064 and1069 to 1071 to reduce the level of AR. AR-full length (AR-FL), AR-FLwith antiandrogen resistance-conferring AR-LSD or other AR mutations,AR-splice variant (AR-SV), and/or amplifications of the AR gene withinthe tumor.

The method may increase radiographic progression free survival (rPFS) ormetastasis-free survival (MFS).

Subjects may have non-metastatic cancer; failed androgen deprivationtherapy (ADT), undergone orchidectomy, or have high or increasingprostate specific antigen (PSA) levels; subjects may be a patient withprostate cancer, advanced prostate cancer, refractory prostate cancer,CRPC patient, metastatic castration resistant prostate cancer (mCRPC)patient, or non-metastatic castration resistant prostate cancer (nmCRPC)patient. In these subjects, the refractory may be enzalutamide resistantprostate cancer. In these subjects, the nmCRPC may be high-risk nmCRPC.Further the subject may be on androgen deprivation therapy (ADT) with orwithout castrate levels of total T.

As used herein, the phrase “a subject suffering from castrationresistant prostate cancer” refers to a subject with at least one of thefollowing characteristics: has been previously treated with androgendeprivation therapy (ADT); has responded to the ADT and currently has aserum PSA >2 ng/mL or >2 ng/mL and representing a 25% increase above thenadir achieved on the ADT; a subject which despite being maintained onandrogen deprivation therapy is diagnosed to have serum PSA progression;a castrate level of serum total testosterone (<50 ng/dL) or a castratelevel of serum total testosterone (<20 ng/dL). The subject may haverising serum PSA on two successive assessments at least 2 weeks apart;been effectively treated with ADT; or has a history of serum PSAresponse after initiation of ADT.

As used herein. the term “serum PSA progression” refers to a 25% orgreater increase in serum PSA and an absolute increase of 2 ng/ml ormore from the nadir; or to serum PSA >2 ng/mL, or >2 ng/mL and a 25%increase above the nadir after the initiation of androgen deprivationtherapy (ADT). The term “nadir” refers to the lowest PSA level while apatient is undergoing ADT.

The term “serum PSA response” refers to at least one of the following:at least 90% reduction in serum PSA value prior to the initiation ofADT; to <10 ng/mL undetectable level of serum PSA (<0.2 ng/mL) at anytime; at least 50% decline from baseline in serum PSA; at least 90%decline from baseline in serum PSA; at least 30% decline from baselinein serum PSA; or at least 10% decline from baseline in serum PSA.

The methods of this invention comprise administering a combination offorms of ADT and a compound of this invention. Forms of ADT include aLHRH agonist. LHRH agonist includes, but is not limited to, leuprolideacetate (Lupron®)(U.S. Pat. Nos. 5,480,656; 5,575,987; 5,631,020;5,643,607; 5,716,640; 5,814,342; 6,036,976 hereby incorporated byreference) or goserelin acetate (Zoladex®) (U.S. Pat. Nos. 7,118,552;7,220,247; 7,500,964 hereby incorporated by reference). Forms of ADTinclude, but are not limited to LHRH antagonists, reversibleantiandrogens, or bilateral orchidectomy. LHRH antagonists include, butare not limited to, degarelix and abarelix. Antiandrogens include, butare not limited to, bicalutamide, flutamide, apalutamide, finasteride,dutasteride, enzalutamide, EPI-001, EPI-506, ARN-509, ODM-201,nilutamide, chlormadinone, abiraterone, or any combination thereof.

The methods of the invention encompass administering at least onecompound of the invention and a lyase inhibitor (e.g., abiraterone).

The term “advanced prostate cancer” refers to metastatic cancer havingoriginated in the prostate, and having widely metastasized to beyond theprostate such as the surrounding tissues to include the seminal vesiclesthe pelvic lymph nodes or bone, or to other parts of the body. Prostatecancer pathologies are graded with a Gleason grading from 1 to 5 inorder of increasing malignancy. Patients with significant risk ofprogressive disease and/or death from prostate cancer should be includedin the definition and any patient with cancer outside the prostatecapsule with disease stages as low as IIB clearly has “advanced”disease. “Advanced prostate cancer” can refer to locally advancedprostate cancer. Similarly, “advanced breast cancer” refers tometastatic cancer having originated in the breast, and having widelymetastasized to beyond the breast to surrounding tissues or other partsof the body such as the liver, brain, lungs, or bone.

The term “refractory” may refer to cancers that do not respond totreatment. E.g., prostate or breast cancer may be resistant at thebeginning of treatment or it may become resistant during treatment.“Refractory cancer” may also be referred to herein as “resistantcancer”.

The term “castration resistant prostate cancer” (CRPC) refers toadvanced prostate cancer that is worsening or progressing while thepatient remains on ADT or other therapies to reduce testosterone, orprostate cancer which is considered hormone refractory, hormone naive,androgen independent or chemical or surgical castration resistant. CRPCmay be the result of AR activation by intracrine androgen synthesis;expression of AR splice variants (AR-SV) that lack ligand binding domain(LSD); or expression of AR-LBD or other AR mutations with potential toresist antagonists. Castration resistant prostate cancer (CRPC) is anadvanced prostate cancer which developed despite ongoing ADT and/orsurgical castration. Castration resistant prostate cancer is defined asprostate cancer that continues to progress or worsen or adversely affectthe health of the patient despite prior surgical castration, continuedtreatment with gonadotropin releasing hormone agonists (e.g.,leuprolide) or antagonists (e.g., degarelix or abarelix), antiandrogens(e.g., bicalutamide, flutamide, apalutamide, enzalutamide, ketoconazole,aminoglutethamide), chemotherapeutic agents (e.g., docetaxel,paclitaxel, cabazitaxel, adriamycin, mitoxantrone, estramustine,cyclophosphamide), kinase inhibitors (imatinib (Gleevec®) or gefitinib(Iressa®), cabozantinib (Cometriq™, also known as XL184)) or otherprostate cancer therapies (e.g., vaccines (sipuleucel-T (Provenge®).GVAX, etc.). herbal (PC-SPES) and lyase inhibitor (abiraterone)) asevidenced by increasing or higher serum levels of prostate specificantigen (PSA), metastasis, bone metastasis, pain, lymph nodeinvolvement, increasing size or serum markers for tumor growth,worsening diagnostic markers of prognosis, or patient condition.

Castration resistant prostate cancer may be defined as hormone naiveprostate cancer. In men with castration resistant prostate cancer, thetumor cells may have the ability to grow in the absence of androgens(hormones that promote the development and maintenance of male sexcharacteristics).

Many early prostate cancers require androgens for growth, but advancedprostate cancers are androgen-independent, or hormone nave.

The term “androgen deprivation therapy” (ADT) may include orchiectomy;administering luteinizing hormone-releasing hormone (LHRH) analogs;administering luteinizing hormone-releasing hormone (LHRH) antagonists;administering 5α-reductase inhibitors; administering antiandrogens;administering inhibitors of testosterone biosynthesis; administeringestrogens; or administering 17α-hydroxylase/C17,20 lyase (CYP17A1)inhibitors. LHRH drugs lower the amount of testosterone made by thetesticles. Examples of LHRH analogs available in the United Statesinclude leuprolide (Lupron®, Viadur®, Eligard®), goserelin (Zoladex®),triptorelin (Trelstar®), and histrelin (Vantas®). Antiandrogens blockthe body's ability to use any androgens. Examples of antiandrogens drugsinclude enzalutamide (Xtandi®), flutamide (Eulexin200 ), apalutamide(Erlcada®), bicalutamide (Casodex®), and nilutamide (Nilandron®).Luteinizing hormone-releasing hormone (LHRH) antagonists includeabarelix (Plenaxis®) or degarelix (Firrnagon®) (approved for use by theFDA in 2008 to treat advanced prostate cancer), 5α-Reductase inhibitorsblock the body's ability to convert testosterone to the more activeandrogen, 5α-dihydrotestosterone (DHT) and include drugs such asfinasteride (Proscar®) and dutasteride (Avodart®). Inhibitors oftestosterone biosynthesis include drugs such as ketoconazole (Nizoral®).Estrogens include diethylstilbestrol or 17β-estradiol.17α-Hydroxylase/C17,20 lyase (CYP17A1) inhibitors include abiraterone(Zytiga®).

The invention encompasses a method of treating antiandrogen-resistantprostate cancer. The antiandrogen may include, but is not limited to,bicalutamide, hydroxyflutamide, flutamide, apalutamide, enzalutamide,darolutamide, or abiraterone.

The invention encompasses a method of treating prostate cancer in asubject in need thereof, wherein said subject has a rearranged AR. ARoverexpressing prostate cancer. castration-resistant prostate cancer,castration-sensitive prostate cancer. AR-V7 expressing prostate cancer,or d567ES expressing prostate cancer, comprising administering to thesubject a therapeutically effective amount of a selective androgenreceptor degrader (SARD) compound, or its isomer, pharmaceuticallyacceptable salt, pharmaceutical product, polymorph, hydrate or anycombination thereof, wherein said SARD compound is represented by thestructure of formula I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VHIB, IXA or IXB, or the compound is at least one of compounds 1001 to1064 and 1069 to 1071.

In one embodiment, the castration-resistant prostate cancer is arearranged AR, AR overexpressing castration-resistant prostate cancer,F876L mutation expressing castration-resistant prostate cancer,F876L_T877A double mutation expressing castration-resistant prostatecancer, AR-V7 expressing castration-resistant prostate cancer, d567ESexpressing castration-resistant prostate cancer, and/orcastration-resistant prostate cancer characterized by intratumoralandrogen synthesis.

In one embodiment, the castration-sensitive prostate cancer is F876Lmutation expressing castration-sensitive prostate cancer, F876L_T877Adouble mutation castration-sensitive prostate cancer, and/orcastration-sensitive prostate cancer characterized by intratumoralandrogen synthesis.

In one embodiment, the treating of castration-sensitive prostate canceris conducted in a non-castrate setting, or as monotherapy, or whencastration-sensitive prostate cancer tumor is resistant to enzalutamide,apalutamide, and/or abiraterone.

The invention encompasses a method of treating AR overexpressingprostate cancer in a subject in need thereof, comprising administeringto the subject a therapeutically effective amount of a selectiveandrogen receptor degrader (SARD) compound, or its isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof. wherein said SARD compound isrepresented by the structure of formula I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071.

The invention encompasses a method of treating castration-resistantprostate cancer in a subject in need thereof, comprising administeringto the subject a therapeutically effective amount of a selectiveandrogen receptor degrader (SARD) compound, or its isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof. wherein said SARD compound isrepresented by the structure of formula I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071. In one embodiment, thecastration-resistant prostate cancer is a rearranged AR, ARoverexpressing castration-resistant prostate cancer, F876L mutationexpressing castration-resistant prostate cancer. F876L_T877A doublemutation expressing castration-resistant prostate cancer. AR-V7expressing castration-resistant prostate cancer, d567ES expressingcastration-resistant prostate cancer, and/or castration-resistantprostate cancer characterized by intratumoral androgen synthesis.

The invention encompasses a method of treating castration-sensitiveprostate cancer in a subject in need thereof, comprising administeringto the subject a therapeutically effective amount of a selectiveandrogen receptor degrader (SARD) compound, or its isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof, wherein said SARD compound isrepresented by the structure of formula I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071. In one embodiment, thecastration-sensitive prostate cancer is F876L mutation expressingcastration-sensitive prostate cancer. F876L_T877A double mutationcastration-sensitive prostate cancer, and/or castration-sensitiveprostate cancer characterized by intratumoral androgen synthesis. In oneembodiment, the treating of castration-sensitive prostate cancer isconducted in a non-castrate setting, or as monotherapy, or whencastration-sensitive prostate cancer tumor is resistant to enzalutamide,apalutamide, and/or abiraterone.

The invention encompasses a method of treating AR-V7 expressing prostatecancer in a subject in need thereof, comprising administering to thesubject a therapeutically effective amount of a selective androgenreceptor degrader (SARD) compound, or its isomer, pharmaceuticallyacceptable salt, pharmaceutical product, polymorph, hydrate or anycombination thereof. wherein said SARD compound is represented by thestructure of formula I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB, or the compound is at least one of compounds 1001 to1064 and 1069 to 1071.

The invention encompasses a method of treating d567ES expressingprostate cancer in a subject in need thereof, comprising administeringto the subject a therapeutically effective amount of a selectiveandrogen receptor degrader (SARD) compound, or its isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof, wherein said SARD compound isrepresented by the structure of formula I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071.

Treatment of Triple Negative Breast Cancer (TNBC)

Triple negative breast cancer (TNBC) is a type of breast cancer lackingthe expression of the estrogen receptor (ER), progesterone receptor(PR), and HER2 receptor kinase. As such, TNBC lacks the hormone andkinase therapeutic targets used to treat other types of primary breastcancers. Correspondingly, chemotherapy is often the initialpharmacotherapy for TNBC. Interestingly, AR is often still expressed inTNBC and may offer a hormone targeted therapeutic alternative tochemotherapy. In ER-positive breast cancer, AR is a positive prognosticindicator as it is believed that activation of AR limits and/or opposesthe effects of the ER in breast tissue and tumors. However, in theabsence of ER, it is possible that AR actually supports the growth ofbreast cancer tumors. Though the role of AR is not fully understood inTNBC, we have evidence that certain TNBC's may be supported by androgenindependent activation of AR-SVs lacking the LBD or androgen-dependentactivation of AR full length. As such, enzalutamide and otherLBD-directed traditional AR antagonists would not he able to antagonizeAR-SVs in these TNBC's. However, SARDs of this invention which arecapable of destroying AR-SVs (see Table 1 and Example 5) through abinding site in the NTD of AR (see Example 9) would be able toantagonize AR in these TNBC's and provide an anti-tumor effect, as shownin Example 8.

Treatment of Kennedy's Disease

Muscle atrophy (MA) is characterized by wasting away or diminution ofmuscle and a decrease in muscle mass. For example, post-polio MA ismuscle wasting that occurs as part of the post-polio syndrome (PPS). Theatrophy includes weakness, muscle fatigue, and pain. Another type of MAis X-linked spinal-bulbar muscular atrophy (SBMA also known as Kennedy'sDisease). This disease arises from a defect in the androgen receptorgene on the X chromosome, affects only males, and its onset is in lateadolescence to adulthood. Proximal limb and bulbar muscle weaknessresults in physical limitations including dependence on a wheelchair insome cases. The mutation results in an extended polyglutamine tract atthe N-terminal domain of the androgen receptor (polyQ AR).

Binding and activation of the polyQ AR by endogeneous androgens(testosterone and DHT) results in unfolding and nuclear translocation ofthe mutant androgen receptor. The androgen-induced toxicity andandrogen-dependent nuclear accumulation of polyQ AR protein seems to becentral to the pathogenesis. Therefore, the inhibition of theandrogen-activated polyQ AR might be a therapeutic option (A. Baniahmad.Inhibition of the androgen receptor by antiandrogens in spinobulbarmuscle atrophy. J. Mol. Neurosci. 2016 58(3), 343-347). These steps arerequired for pathogenesis and result in partial loss of transactivationfunction (i.e., an androgen insensitivity) and a poorly understoodneuromuscular degeneration. Peripheral polyQ AR anti-sense therapyrescues disease in mouse models of SBMA (Cell Reports 7, 774-784, May 8,2004). Further support of use antiandrogen comes in a report in whichthe antiandrogen flutamide protects male mice from androgen-dependenttoxicity in three models of spinal bulbar muscular atrophy (Renier K J,Troxell-Smith S M, Johansen J A, Katsuno M, Adachi H, Sobue G, Chua J P,Sun Kim H, Lieberman A P, Breedlove S M, Jordan C L. Endocrinology 2014,155(7), 2624-2634). These steps are required for pathogenesis and resultin partial loss of transactivation function (i.e., an androgeninsensitivity) and a poorly understood neuromuscular degeneration.Currently there are no disease-modifying treatments but rather onlysymptom directed treatments. Efforts to target the polyQ AR as theproximal mediator of toxicity by harnessing cellular machinery topromote its degradation hold promise for therapeutic intervention.

Selective androgen receptor degraders such as those reported herein hindto, inhibit transactivation, and degrade all androgen receptors testedto date (full length, splice variant, antiandrogen resistance mutants,etc.), indicating that they are promising leads for treatment diseaseswhose pathogenesis is androgen-dependent such as SBMA.

The invention encompasses methods of treating Kennedy's diseasecomprising administering a therapeutically effective amount of acompound of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB or the compound is at least one of compounds 1001 to1064 and 1069 to 1071.

The term “androgen receptor dependent disease or condition” refers todiseases or conditions that have pathological origins or propogated bythe altered, increased, dysregulated, or abberant activity of anandrogen receptor. In some embodiments, the androgen receptor is afull-length androgen receptor. In another embodiment, the androgenreceptor is a wildtype full-length androgen receptor (AR-FL). In anotherembodiment, the androgen receptor is a point mutation of the full-lengthandrogen receptor. In another embodiment, the androgen receptor is apolyQ polymorph. In another embodiment, the androgen receptor is asplice-variant of the androgen receptor (AR-SV). In another embodiment,the androgen receptor is any of the above or a combination thereof. Inanother embodiment, the androgen receptor is any of the above and isadditionally overexpressed. In another embodiment, the androgen receptoris any of the above and further recombined with another gene to form afusion protein. Examples of common AR fusion proteins include but arenot limited to TMPRSS2 or ETS-family of transcription factors. In someembodiments, the androgen receptor is any of the above and presence in apathologically changed cellular milicau. In another embodiment, thealtered. increased, dysregulated or abberant activity of an androgenreceptor is caused by endogeneous androgens acting at the androgenreceptor. In another embodiment, the altered, increased. dysregulated,or abberant activity of an androgen receptor is caused by exogeneouslyadministered compounds acting at the androgen receptor. In anotherembodiment, the altered, increased, dysregulated, or abberant activityof an androgen receptor is ligand-independent. In another embodiment,the ligand-independent activity is caused by the constitutive activityof the androgen receptor. In another embodiment, the ligand-independentactivity is caused by constitutively active mutants of the androgenreceptor. In another embodiment, the ligand-independent activity iscaused by pathologic cellular milicau. In another embodiment, theseandrogen receptor dependent diseases and conditions are improved by theadministration of androgen receptor antagonists. In another embodiment,these androgen receptor dependent diseases and conditions are improvedby the administration of androgen deprivation therapies (ADT) asdescribed herein. In another embodiment, these androgen receptordependent diseases and conditions are made worse by the administrationof androgen receptor agonists. In another embodiment, these androgenreceptor dependent diseases and conditions are improved by decreasingandrogen receptor expression by biochemical treatments. In anotherembodiment, these androgen receptor dependent diseases and conditions amthe result of hormonal imbalances. In another embodiment, the hormonalimbalance in a subject is a result of ageing, or in the otherembodiments, the result of disease. In another embodiment, theseandrogen receptor dependent diseases and conditions are responsive tothe administration of androgen receptor antagonists such asanti-androgens. In another embodiment, these androgen receptor dependentdiseases and conditions are conditions, diseases, or disorders that aremodulated by or whose pathogenesis is dependent upon the activity of theandrogen receptor.

In some embodiments, the androgen receptor dependent diseases andconditions are improved by administration of the selective androgenreceptor degraders of the invention. In some embodiments, the benefit ofselective androgen receptor degraders of the invention is theirdegradation of at least one form of the androgen receptor. In someembodiments, the benefit of selective androgen receptor degraders of theinvention is their inhibition of at least one form of the androgenreceptor. In some embodiments, the benefit of selective androgenreceptor degraders of the invention is their degradation and inhibitionof at least one form of the androgen receptor.

Many examples of androgen receptor dependent diseases and conditions aredescribed herein, and these include but are not limited to prostatecancers, breast cancers, hormone-dependent cancers, hormone-independentcancers. AR-expressing cancers, and precursors to hormone-dependentcancers as are each described in detail herein below; dermatologicaldisorders, hormonal conditions of a male or hormonal conditions of afemale as are each described in detail herein below; androgeninsufficiency syndromes as are described in detail below; uterinefibroids, Kennedy's disease (SBMA), amyotrophic lateral sclerosis (ALS),abdominal aortic aneurysm (AAA), improving wound healing, sexualperversion, hypersexuality, paraphilias, androgen psychosis, andvirilization and the like.

As used herein, the term “androgen receptor associated conditions” or“androgen sensitive diseases or disorders” or “androgen-dependentdiseases or disorders” are conditions, diseases, or disorders that aremodulated by or whose pathogenesis is dependent upon the activity of theandrogen receptor. The androgen receptor is expressed in most tissues ofthe body however it is overexpressed in inter alia, the prostate andskin. ADT has been the mainstay of prostate cancer treatment for manyyears, and SARDs may also be useful in treating various prostatecancers, benign prostatic hypertrophy, prostamegaly, and other maladiesof the prostate.

The invention encompasses methods of treating benign prostatichypertrophy comprising administering a therapeutically effective amountof at least one compound of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071.

The invention encompasses methods of treating prostamegaly comprisingadministering a therapeutically effective amount of at least onecompound of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB or the compound is at least one of compounds 1001 to1064 and 1069 to 1071.

The invention encompasses methods of treating hyperproliferativeprostatic disorders and diseases comprising administering atherapeutically effective amount of a compound of formulas I-IX, IA, IB,IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or the compoundis at least one of compounds 1001 to 1064 and 1069 to 1071.

The effect of the AR on the skin is apparent in the gender dimorphismand puberty related dermatological problems common to teens and earlyadults. The hyperandrogenism of puberty stimulates terminal hair growth,sebum production, and predisposes male teens to acne, acne vulgaris,seborrhea, excess sebum, hidradenitis suppurativa, hirsutism,hypertrichosis, hyperpilosity, androgenic alopecia, male patternbaldness, and other dermatological maladies. Although antiandrogenstheoretically should prevent the hyperandrogenic dermatological diseasesdiscussed, they are limited by toxicities, sexual side effects, and lackof efficacy when topically applied. The SARDs of this invention potentlyinhibit ligand-dependent and ligand-independent AR activation, and (insome cases) have short biological half-lives in the serum, suggestingthat topically formulated SARDs of this invention could he applied tothe areas affected by acne, seborrheic dermatitis, and/or hirsutismwithout risk of systemic side effects.

The invention encompasses methods of treating acne, acne vulgaris,seborrhea, seborrheic dermatitis, hidradenitis supporativa, hirsutism,hypertrichosis, hyperpilosity, or alopecia comprising administering atherapeutically effective amount of a compound of formulas I-IX, IA, IB,IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or any ofcompounds 1001 to 1064 and 1069 to 1071.

The compounds and/or compositions described herein may be used fortreating hair loss, alopecia, androgenic alopecia, alopecia areata,alopecia secondary to chemotherapy, alopecia secondary to radiationtherapy, alopecia induced by scarring or alopecia induced by stress.Generally “hair loss” or “alopecia” refers to baldness as in the verycommon type of male-pattern baldness. Baldness typically begins withpatch hair loss on the scalp and sometimes progresses to completebaldness and even loss of body hair. Hair loss affects both males andfemales.

The invention encompasses methods of treating androgenic alopeciacomprising administering a therapeutically effective amount of acompound of formula I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB, or any of compounds 1001 to 1064 and 1069 to 1071.

The invention encompasses methods of treating, suppressing, reducing theincidence, reducing the severity, or inhibiting the progression of ahormonal condition in a male in need thereof, comprising administeringto the subject a therapeutically effective amount of a selectiveandrogen receptor degrader (SARD) compound, or its isomer,pharmaceutically acceptable salt, pharmaceutical product, polymorph,hydrate or any combination thereof, wherein said SARD compound isrepresented by the structure of formula I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071.

In one embodiment, the condition is hypergonadism, hypersexuality,sexual dysfunction, gynecomastia, precocious puberty in a male,alterations in cognition and mood, depression, hair loss,hyperandrogenic dermatological disorders, pre-cancerous lesions of theprostate, benign prostate hyperplasia, prostate cancer and/or otherandrogen-dependent cancers.

SARDs of this invention may also be useful in the treatment of hormonalconditions in females which can have hyperandrogenic pathogenesis suchas precocious puberty, early puberty, dysmenorrhea, amenorrhea,multilocular uterus syndrome, endometriosis, hysteromyoma, abnormaluterine bleeding, early menarche, fibrocystic breast disease, fibroidsof the uterus, ovarian cysts, polycystic ovary syndrome, pre-eclampsia,eclampsia of pregnancy, preterm labor, premenstrual syndrome, and/orvaginal dryness.

The invention encompasses methods of treating precocious puberty orearly puberty, dysmenorrhea or amenorrhea, multilocular uterus syndrome,endometriosis, hysteromyoma, abnormal uterine bleeding, hyper-androgenicdiseases (such as polycystic ovary syndrome (PCOS)), fibrocystic breastdisease, fibroids of the uterus, ovarian cysts, polycystic ovarysyndrome, pre-eclampsia, eclampsia of pregnancy, preterm labor,premenstrual syndrome, or vaginal dryness comprising administering atherapeutically effective amount of a compound of formulas I-IX, IA, IB,IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or any ofcompounds 1001 to 1064 and 1069 to 1071.

SARDs of this invention may also Find utility in treatment of sexualperversion, hypersexuality, paraphilias, androgen psychosis,virilization, androgen insensitivity syndromes CAIS) (such as completeAIS (CAIS) and partial AIS (PAIS)), and improving ovulation in ananimal.

The invention encompasses methods of treating sexual perversion,hypersexuality, paraphilias, androgen psychosis, virilization androgen,insensitivity syndromes, increasing or modulating or improving ovulationcomprising administering a therapeutically effective amount of acompound of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB, or any of compounds 1001 to 1064 and 1069 to 1071.

SARDs of this invention may also be useful for treatinghormone-dependent cancers such as prostate cancer, breast cancer,testicular cancer, ovarian cancer, hepatocellular carcinoma, urogenitalcancer, etc. In another embodiment, the breast cancer is triple negativebreast cancer. Further, local or systemic SARD administration may beuseful for treatment of precursors of hormone-dependent cancers such asprostatic intraepithelial neoplasia (PIN) and atypical small acinarproliferation (ASAP).

The invention encompasses methods of treating breast cancer, testicularcancer, uterine cancer, ovarian cancer, urogenital cancer, precursors ofprostate cancer, or AR related or AR expressing solid tumors, comprisingadministering a therapeutically effective amount of a compound offormulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXAor IXB or the compound is at least one of compounds 1001 to 1064 and1069 to 1071. A precursor of prostate cancers may be prostaticintraepithelial neoplasia (PIN) or atypical small acinar proliferation(ASAP). The tumor may be hepatocellular carcinoma (HCC) or bladdercancer. Serum testosterone may be positively linked to the developmentof HCC. Based on epidemiologic, experimental observations, and notablythe fact that men have a substantially higher risk of bladder cancerthan women, androgens and/or the AR may also play a role in bladdercancer initiation.

Although traditional antiandrogens such as enzalutamide, bicalutamideand flutamide and androgen deprivation therapies (ADT) such asleuprolide were approved for use in prostate cancer, there issignificant evidence that antiandrogens could also be used in a varietyof other hormone-dependent and hormone-independent cancers. For example,antiandrogens may be used in a wide variety of AR-expressing cancers asdescribed below. For example, antiandrogens have been successfullytested in breast cancer (enzalutamide: Breast Cancer Res (2014) 16(1):R7), non-small cell lung cancer (shRNAi AR), renal cell carcinoma(ASC-J9), partial androgen insensitivity associated malignancies such asgonadal tumors and seminoma, advanced pancreatic cancer (World J.Gastroenterology 20(29):9229), cancer of the ovary, fallopian tubes, orperitoneum, cancer of the salivary gland (Head and Neck (2016) 38:724-731; ADT was tested in AR-expressing recurrent/metastatic salivarygland cancers and was confirmed to have benefit on progression freesurvival and overall survival endpoints), bladder cancer (Oncotarget 6(30): 29860-29876); Int J Endocrinol (2015), Article ID 384860),pancreatic cancer, lymphoma (including mantle cell), and hepatocellularcarcinoma. Use of a more potent antiandrogen such as a SARD in thesecancers may treat the progression of these and other cancers. Othercancers may also benefit from SARD treatment such as testicular cancer,uterine cancer, ovarian cancer, urogenital cancer, breast cancer, braincancer, skin cancer, lymphoma, liver cancer, renal cancer, osteosarcoma,pancreatic cancer, endometrial cancer, lung cancer, non-small cell lungcancer (NSCLC), colon cancer, perianal adenoma, or central nervoussystem cancer.

SARDs of this invention may also be useful for treating other cancerscontaining AR such as breast, brain, skin, ovarian, bladder, lymphoma,liver, kidney, pancreas, endometrium, lung (e.g., NSCLC), colon,perianal adenoma, osteosarcoma, CNS, melanoma, hypercalcemia ofmalignancy and metastatic bone disease, etc.

Thus, the invention encompasses methods of treating hypercalcemia ofmalignancy, metastatic hone disease, brain cancer, skin cancer, bladdercancer, lymphoma, liver cancer, renal cancer, osteosarcoma, pancreaticcancer, endometrial cancer, lung cancer, central nervous system cancer,gastric cancer, colon cancer, melanoma, amyotrophic lateral sclerosis(ALS), and/or uterine fibroids comprising administering atherapeutically effective amount of a compound of formulas I IX, IA, IB,IC, ID, IIA, DB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or any ofcompounds 1001 to 1064 and 1069 to 1071. The lung cancer may benon-small cell lung cancer (NSCLC).

SARDs of this invention may also be useful for the treating ofnon-hormone-dependent cancers. Non-hormone-dependent cancers includeliver, salivary duct. etc.

In another embodiment, the SARDs of this invention are used for treatinggastric cancer. In another embodiment, the SARDs of this invention areused for treating salivary duct carcinoma. In another embodiment, theSARDs of this invention are used for treating bladder cancer. In anotherembodiment, the SARDs of this invention are used for treating esophagealcancer. In another embodiment, the SARDs of this invention are used fortreating pancreatic cancer. In another embodiment, the SARDs of thisinvention are used for treating colon cancer. In another embodiment, theSARDs of this invention are used for treating non-small cell lungcancer. In another embodiment, the SARDs of this invention are used fortreating renal cell carcinoma.

AR plays a role in cancer initiation in hepatocellular carcinoma (HCC).Therefore, targeting AR may be an appropriate treatment for patientswith early stage HCC. In late-stage HCC disease, there is evidence thatmetastasis is suppressed by androgens. In another embodiment, the SARDsof this invention are used for treating hepatocellular carcinoma (HCC).

Locati et al. in Head & Neck, 2016, 724-731 demonstrated the use ofandrogen deprivation therapy (ADT) in AR-expressing recurrent/metastaticsalivary gland cancers and confirmed improved progression free survivaland overall survival endpoints with ADT. In another embodiment, theSARDs of this invention are used for treating salivary gland cancer.

Kawahara et al. in Oncotarget. 2015, Vol 6 (30), 29860-29876demonstrated that ELK1 inhibition, together with AR inactivation, hasthe potential of being a therapeutic approach for bladder cancer. McBethet al. Int J Endocrinology, 2015, Vol 2015, Article ID 384860 suggestedthat the combination of antiandrogen therapy plus glucocorticoids astreatment of bladder cancer as this cancer is believed to have aninflammatory etiology. In another embodiment, the SARDs of thisinvention are used for treating bladder cancer, optionally incombination with glucocorticoids.

Abdominal Aortic Aneurysm (AAA)

An abdominal aortic aneurysm (AAA) is an enlarged area in the lower partof the aorta, the major blood vessel that supplies blood to the body.The aorta, about the thickness of a garden hose, runs from your heartthrough the center of your chest and abdomen. Because the aorta is thebody's main supplier of blood, a ruptured abdominal aortic aneurysm cancause life-threatening bleeding. Depending on the size and the rate atwhich your abdominal aortic aneurysm is growing. treatment may vary fromwatchful waiting to emergency surgery. Once an abdominal aortic aneurysmis found, doctors will closely monitor it so that surgery can be plannedif it is necessary. Emergency surgery for a ruptured abdominal aorticaneurysm can be risky. AR blockade (pharmacologic or genetic) reducesAAA. Davis et al. (Davis J P, Salmon M, Pope N H, Lu G, Su G, Meher A.Ailawadi G. Upchurch G R Jr. 7 Vasc Surg (2016) 63(6):1602-1612) showedthat flutamide (50 mg/kg) or ketoconazole (150 mg/kg) attenuated AAAinduced by porcine pancreatic elastase (0.35 U/mL) by 84.2% and 91.5%compared to vehicle (121%). Further AR mice showed attenuated AAA growth(64.4%) compared to wildtype (both treated with elastase).Correspondingly, administration of a SARD to a patient suffering from anAAA may help reverse, treat or delay progression of AAA to the pointwhere surgery is needed.

Treatment of Wounds

Wounds and/or ulcers are normally found protruding from the skin or on amucosal surface or as a result elan infarction in an organ. A wound maybe a result of a soft tissue defect or a lesion or of an underlyingcondition. The term “wound” denotes a bodily injury with disruption ofthe normal integrity of tissue structures, sore, lesion, necrosis,and/or ulcer. The term “sore” refers to any lesion of the skin or mucousmembranes and the term “ulcer” refers to a local defect, or excavation,of the surface of an organ or tissue, which is produced by the sloughingof necrotic tissue. “Lesion” generally includes any tissue defect.“Necrosis” refers to dead tissue resulting from infection, injury,inflammation, or infarctions. All of these are encompassed by the term“wound,” which denotes any wound at any particular stage in the healingprocess including the stage before any healing has initiated or evenbefore a specific wound like a surgical incision is made (prophylactictreatment).

Examples of wounds which can he treated in accordance with the presentinvention are aseptic wounds, contused wounds, incised wounds, laceratedwounds, non-penetrating wounds (i.e. wounds in which there is nodisruption of the skin but there is injury to underlying structures),open wounds, penetrating wounds, perforating wounds, puncture wounds,septic wounds, subcutaneous wounds, etc. Examples of sores include, butare not limited to, bed sores, canker sores, chrome sores, cold sores,pressure sores, etc. Examples of ulcers include, but are not limited to,peptic ulcer, duodenal ulcer, gastric ulcer, gouty ulcer, diabeticulcer, hypertensive ischemic ulcer, stasis ulcer, ulcus cruris (venousulcer), sublingual ulcer, submucous ulcer, symptomatic ulcer, trophiculcer, tropical ulcer, veneral ulcer, e.g., caused by gonorrhoea(including urethritis, endocervicitis and proctitis). Conditions relatedto wounds or sores which may be successfully treated according to theinvention include, but are not limited to, bums, anthrax, tetanus, gasgangrene, scalatina, erysipelas, sycosis barbae, folliculitis, impetigocontagiosa, impetigo bullosa, etc. It is understood, that there may bean overlap between the use of the terms “wound” and “ulcer,” or “wound”and “sore” and, furthermore, the terms are often used at random.

The kinds of wounds to be treated according to the invention includealso: i) general wounds such as, e.g., surgical, traumatic, infectious,ischemic, thermal, chemical and bullous wounds; ii) wounds specific forthe oral cavity such as, e.g., post-extraction wounds, endodontic woundsespecially in connection with treatment of cysts and abscesses, ulcersand lesions of bacterial, viral or autoimmunological origin, mechanical,chemical, thermal, infectious and lichenoid wounds; herpes ulcers,stomatitis aphthosa, acute necrotising ulcerative gingivitis and burningmouth syndrome are specific examples; and iii) wounds on the skin suchas, e.g., neoplasm, hums (e.g. chemical, thermal), lesions (bacterial,viral, autoimmunological), bites and surgical incisions. Another way ofclassifying wounds is by tissue loss, where: i) small tissue loss (dueto surgical incisions, minor abrasions, and minor bites) or ii)significant tissue loss. The latter group includes ischemic ulcers,pressure sores, fistulae, lacerations, severe bites, thermal burns anddonor site wounds (in soft and hard tissues) and infarctions. Otherwounds include ischemic ulcers, pressure sores. fistulae. severe bites,thermal hums, or donor site wounds.

Ischemic ulcers and pressure sores are wounds, which normally only healvery slowly and especially in such cases an improved and more rapidhealing is of great importance to the patient. Furthermore, the costsinvolved in the treatment of patients suffering from such wounds aremarkedly reduced when the healing is improved and takes place morerapidly.

Donor site wounds are wounds which e.g. occur in connection with removalof hard tissue from one part of the body to another part of the bodye.g. in connection with transplantation. The wounds resulting from suchoperations are very painful and an improved healing is therefore mostvaluable.

In one case, the wound to he treated is selected from the groupconsisting of aseptic wounds, infarctions, contused wounds, incisedwounds, lacerated wounds, non-penetrating wounds, open wounds,penetrating wounds, perforating wounds, puncture wounds, septic wounds,and subcutaneous wounds.

The invention encompasses methods of treating a subject suffering from awound comprising administering to the subject a therapeuticallyeffective amount of a compound of formulas I-IX, IA, IB, IC, ID, IIA,IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB, or the compound is at leastone of compounds 1001 to 1064 and 1069 to 1071; or pharmaceuticallyacceptable salt thereof, or a pharmaceutical composition thereof.

The invention encompasses methods of treating a subject suffering from aburn comprising administering to the subject a therapeutically effectiveamount of a compound of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA or IXB, or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071; or pharmaceutically acceptablesalt thereof, or a pharmaceutical composition thereof.

The term “skin” is used in a very broad sense embracing the epidermallayer of the skin and in those cases where the skin surface is more orless injured also the dermal layer of the skin. Apart from the stratumcorneum, the epidermal layer of the skin is the outer (epithelial) layerand the deeper connective tissue layer of the skin is called the dermis.

Since the skin is the most exposed part of the body, it is particularlysusceptible to various kinds of injuries such as, e.g., ruptures, cuts,abrasions, bums and frostbites or injuries arising from variousdiseases. Furthermore. much skin is often destroyed in accidents.However, due to the important barrier and physiologic function of theskin, the integrity of the skin is important to the well-being of theindividual, and any breach or rupture represents a threat that must bemet by the body in order to protect its continued existence.

Apart from injuries on the skin, injuries may also be present in allkinds of tissues (i.e. soft and hard tissues). Injuries on soft tissuesincluding mucosal membranes and/or skin are especially relevant inconnection with the present invention.

Healing of a wound on the skin or on a mucosal membrane undergoes aseries of stages that results either in repair or regeneration of theskin or mucosal membrane. In recent years. regeneration and repair havebeen distinguished as the two types of healing that may occur.Regeneration may be defined as a biological process whereby thearchitecture and function of lost tissue are completely renewed. Repair,on the other hand, is a biological process whereby continuity ofdisrupted tissue is restored by new tissues which do not replicate thestructure and function of the lost ones.

The majority of wounds heal through repair, meaning that the new tissueformed is structurally and chemically unlike the original tissue (scartissue). In the early stage of the tissue repair, one process which isalmost always involved is the formation of a transient connective tissuein the area of tissue injury. This process starts by formation of a newextracellular collagen matrix by fibroblasts. This new extracellularcollagen matrix is then the support for a connective tissue during thefinal healing process. The final healing is, in most tissues, a scarformation containing connective tissue. In tissues which haveregenerative properties, such as, e.g., skin and bone, the final healingincludes regeneration of the original tissue. This regenerated tissuehas frequently also some scar characteristics, e.g, a thickening of ahealed bone fracture.

Under normal circumstances, the body provides mechanisms for healinginjured skin or mucosa in order to restore the integrity of the skinharrier or the mucosa. The repair process for even minor ruptures orwounds may take a period of time extending from hours and days to weeks.However, in ulceration, the healing can be very slow and the wound maypersist for an extended period of time, i.e. months or even years.

Burns are associated with reduced testosterone levels, and hypogonadismis associated with delayed wound healing. The invention encompassesmethods for treating a subject suffering from a wound or a burn byadministering at least one SARD compound according to this invention.The SARD may promote resolving of the burn or wound, participates in thehealing process of a burn or a wound, or, treats a secondarycomplication of a burn or wound.

1003251 The treatment of burns or wounds may further use at least onegrowth factor such as epidermal growth factor (EGF), transforming growthfactor-α (TGF-α), platelet derived growth factor (PDGF), fibroblastgrowth factors (FGFs) including acidic fibroblast growth factor (α-FGF)and basic fibroblast growth factor (β-FGF), transforming growth factor-β(TGF-β) and insulin like growth factors (IGF-1 and IGF-2), or anycombination thereof. which promote wound healing.

Wound healing may be measured by many procedures known in the art,including, but not limited to, wound tensile strength, hydroxyproline orcollagen content, procollagen expression, or re-epithelialization. As anexample, a SARD as described herein may be administered orally ortopically at a dosage of about 0.1-100 mg per day. Therapeuticeffectiveness is measured as effectiveness in enhancing wound healing ascompared to the absence of the SARD compound. Enhanced wound healing maybe measured by known techniques such as decrease in healing time,increase in collagen density, increase in hydroxyproline, reduction incomplications, increase in tensile strength, and increased cellularityof scar tissue.

The term “reducing the pathogenesis” is to be understood to encompassreducing tissue damage, or organ damage associated with a particulardisease, disorder or condition. The term may include reducing theincidence or severity of an associated disease, disorder or condition,with that in question or reducing the number of associated diseases,disorders or conditions with the indicated, or symptoms associatedthereto.

Pharmaceutical Compositions

The compounds of the invention may be used in pharmaceuticalcompositions. As used herein, “pharmaceutical composition” means eitherthe compound or pharmaceutically acceptable salt of the activeingredient with a pharmaceutically acceptable carrier or diluent. A“therapeutically effective amount” as used herein refers to that amountwhich provides a therapeutic effect for a given indication andadministration regimen.

As used herein. the term “administering” refers to bringing a subject incontact with a compound of the present invention. As used herein,administration can be accomplished in vitro, i.e. in a test tube, or invivo, i.e. in cells or tissues of living organisms, for example humans.The subjects may be a male or female subject or both.

Numerous standard references are available that describe procedures forpreparing various compositions or formulations suitable foradministration of the compounds of the invention. Examples of methods ofmaking formulations and preparations can he found in the Handbook ofPharmaceutical Excipients, American Pharmaceutical Association (currentedition); Pharmaceutical Dosage Forms: Tablets (Lieberman, Lachman andSchwartz, editors) current edition, published by Marcel Dekker. Inc., aswell as Remington's Pharmaceutical Sciences (Arthur Osol. editor).1553-1593 (current edition).

The mode of administration and dosage form are closely related to thetherapeutic amounts of the compounds or compositions which are desirableand efficacious for the given treatment application.

The pharmaceutical compositions of the invention can be administered toa subject by any method known to a person skilled in the art. Thesemethods include, but are not limited to, orally, parenterally,intravascularly, paracancerally, transmucosally, transdermally,intramuscularly, intranasally, intravenously, intradermally,subcutaneously, sublingually, intraperitoneally, intraventricularly,intracranially, intravaginally, by inhalation, rectally, orintratumorally. These methods include any means in which the compositioncan be delivered to tissue (e.g., needle or catheter). Alternatively, atopical administration may be desired for application to dermal, ocular,or mucosal surfaces. Another method of administration is via aspirationor aerosol formulation. The pharmaceutical compositions may beadministered topically to body surfaces, and are thus formulated in aform suitable for topical administration. Suitable topical formulationsinclude gels, ointments, creams, lotions, drops and the like. Fortopical administrations, the compositions are prepared and applied assolutions, suspensions, or emulsions in a physiologically acceptablediluent with or without a pharmaceutical carrier.

Suitable dosage forms include, but are not limited to, oral, rectal,sub-lingual, mucosal, nasal, ophthalmic, subcutaneous, intramuscular,intravenous, transdermal, spinal, intrathecal. intra-articular,intra-arterial, sub-arachinoid, bronchial, lymphatic, and intra-uterileadministration, and other dosage forms for systemic delivery of activeingredients. Depending on the indication, formulations suitable for oralor topical administration are preferred.

Topical Administration: The compounds of formulas I-IX, IA, IB, IC, ID,IIA, IIB, VIIA, VIIB, VIIIA, VMS, IXA or IXB or the compound is at leastone of compounds 1001 to 1064 and 1069 to 1071 may be administeredtopically. As used herein, “topical administration” refers toapplication of the compounds of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071 (and optional carrier) directlyto the skin and/or hair. The topical composition can be in the form ofsolutions, lotions, salves, creams, ointments, liposomes, sprays, gels,foams, roller sticks, and any other formulation routinely used indermatology.

Topical administration is used for indications found on the skin, suchas hirsutism, alopecia, acne, and excess sebum. The dose will vary, butas a general guideline, the compound will he present in adermatologically acceptable carrier in an amount of from about 0.01 to50 w/w %, and more typically from about 0.1 to 10 w/w %. Typically, thedermatological preparation will be applied to the affected area from 1to 4 times daily. “Dermatologically acceptable” refers to a carrierwhich may be applied to the skin or hair, and which will allow the drugto diffuse to the site of action. More specifically “site of action”, itrefers to a site where inhibition of androgen receptor or degradation ofthe androgen receptor is desired.

The compounds of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VHS,VIIIA, VIIIB, IXA or IXB, or the compound is at least one of compounds1001 to 1064 and 1069 to 1071 may be used topically to relieve alopecia,especially androgenic alopecia. Androgens have a profound effect on bothhair growth and hair loss. In most body sites, such as the beard andpubic skin, androgens stimulate hair growth by prolonging the growthphase of the hair cycle (anagen) and increasing follicle size. Hairgrowth on the scalp does not require androgens hut, paradoxically,androgens are necessary for the balding on the scalp in geneticallypredisposed individuals (androgenic alopecia) where there is aprogressive decline in the duration of anagen and in hair follicle size.Androgenic alopecia is also common in women where it usually presents asa diffuse hair loss rather than showing the patterning seen in men.

While the compounds of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA,VIIB, VIIIA, VIIIB, IXA or IXB or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071 will most typically be used toalleviate androgenic alopecia, the compounds may be used to alleviateany type of alopecia. Examples of non-androgenic alopecia include, butare not limited to, alopecia areata, alopecia due to radiotherapy orchemotherapy, scarring alopecia, or stress related alopecia.

The compounds of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA or IXB or the compound is at least one of compounds1001 to 1064 and 1069 to 1071 can be applied topically to the scalp andhair to prevent, or treat balding. Further, the compound of formulasI-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB orthe compound is at least one of compounds 1001 to 1064 and 1069 to 1071can be applied topically in order to induce or promote the growth orregrowth of hair on the scalp.

The invention also encompasses topically administering a compound offormula I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA orIXB or the compound is at least one of compounds 1001 to 1064 and 1069to 1071 to treat or prevent the growth of hair in areas where such hairgrowth in not desired. One such use will be to alleviate hirsutism.Hirsutism is excessive hair growth in areas that typically do not havehair (e.g., a female face). Such inappropriate hair growth occurs mostcommonly in women and is frequently seen at menopause. The topicaladministration of the compounds of formulas I-IX, IA, IB, IC, ID, IIA,IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or the compound is at leastone of compounds 1001 to 1064 and 1069 to 1071 will alleviate thiscondition leading to a reduction, or elimination of this inappropriate,or undesired, hair growth.

The compounds of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB,VIIIA, VIIIB, IXA or IXB or the compound is at least one of compounds1001 to 1064 and 1069 to 1071 may also be used topically to decreasesebum production. Sebum is composed of triglycerides, wax esters, fattyacids, sterol esters and squalene. Sebum is produced in the acinar cellsof the sebaceous glands and accumulates as these cells age. Atmaturation, the acinar cells lyse, releasing sebum into the luminal ductso that it may be deposited on the surface of the skin.

In some individuals, an excessive quantity of sebum is secreted onto theskin. This can have a number of adverse consequences. It can exacerbateacne, since sebum is the primary food source for Propionbacterium acnes,the causative agent of acne. It can cause the skin to have a greasyappearance. typically considered cosmetically unappealing.

Formation of sebum is regulated by growth factors and a variety ofhormones including androgens. The cellular and molecular mechanism bywhich androgens exert their influence on the sebaceous gland has notbeen fully elucidated. However, clinical experience documents the impactandrogens have on sebum production. Sebum production is significantlyincreased during puberty, when androgen levels are their highest. Thecompounds of formulas I-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA,VIIIB, IXA or IXB or the compound is at least one of compounds 1001 to1064 and 1069 to 1071 inhibit the secretion of sebum and thus reduce theamount of sebum on the surface of the skin. The compounds of formulasI-IX, IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB orthe compound is at least one of compounds 1001 to 1064 and 1069 to 1071can be used to treat a variety of dermal diseases such as acne orseborrheic dermatitis.

In addition to treating diseases associated with excess sebumproduction, the compounds of formulas I-IX, IA, IB, IC, ID, IIA, IIB,VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or the compound is at least one ofcompounds 1001 to 1064 and 1069 to 1071 can also be used to achieve acosmetic effect. Some consumers believe that they are afflicted withoveractive sebaceous glands. They feel that their skin is oily and thusunattractive. These individuals may use the compounds of formulas I-IX,IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or thecompound is at least one of compounds 1001 to 1064 and 1069 to 1071 todecrease the amount of sebum on their skin. Decreasing the secretion ofsebum will alleviate oily skin in indviduals afflicted with suchconditions.

To treat these topical indications, the invention encompasses cosmeticor pharmaceutical compositions (such as dermatological compositions),comprising at least one of the compounds of formulas I-IX, IA, IB, IC,ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or the compound is atleast one of compounds 1001 to 1064 and 1069 to 1071. Suchdermatological compositions will contain from 0.001% to 10% w/w% of thecompound(s) in admixture with a dermatologically acceptable carrier, andmore typically, from 0.1 to 5 w/w % of the compounds. Such compositionswill typically he applied from 1 to 4 times daily. The reader'sattention is directed to Remington's Pharmaceutical Science, Edition 17.Mark Publishing Co. Easton, Pa. for a discussion of how to prepare suchformulations.

The compositions of the invention may also include solid preparationssuch as cleansing soaps or bars. These compositions are preparedaccording to methods known in the art.

Formulations such as aqueous, alcoholic, or aqueous-alcoholic solutions,or creams, gels, emulsions or mousses, or aerosol compositions with apropellant may be used to treat indications that arise where hair ispresent. Thus, the composition can also be a hair care composition. Suchhair care compositions include, but are not limited to, shampoo, ahair-setting lotion, a treating lotion, a styling cream or gel, a dyecomposition, or a lotion or gel for preventing hair loss. The amounts ofthe various constituents in the dermatological compositions are thoseconventionally used in the Fields considered.

Medicinal and cosmetic agents containing the compounds of formulas I-IX,IA, IB, IC, ID, IIA, IIB, VIIA, VIIB, VIIIA, VIIIB, IXA or IXB or thecompound is at least one of compounds 1001 to 1064 and 1069 to 1071 willtypically he packaged for retail distribution (i.e., an article ofmanufacture). Such articles will be labeled and packaged in a manner toinstruct the patient how to use the product. Such instructions willinclude the condition to be treated, duration of treatment, dosingschedule, etc.

Antiandrogens, such as finasteride or flutamide, have been shown todecrease androgen levels or block androgen action in the skin to someextent but suffer from undesirable systemic effects. An alternativeapproach is to topically apply a selective androgen receptor degrader(SARD) compound to the affected areas. Such SARD compound would exhibitpotent but local inhibition of AR activity, and local degradation of theAR. would not penetrate to the systemic circulation of the subject, orwould be rapidly metabolized upon entry into the blood, limitingsystemic exposure.

To prepare such pharmaceutical dosage forms, the active ingredient maybe mixed with a pharmaceutical carrier according to conventionalpharmaceutical compounding techniques. The carrier may take a widevariety of forms depending on the form of preparation desired foradministration.

As used herein “pharmaceutically acceptable carriers or diluents” arewell known to those skilled in the art. The carrier or diluent may be asolid carrier or diluent for solid formuations, a liquid carrier ordiluent for liquid formulations, or mixtures thereof.

Solid carriers/diluents include, but are not limited to, a gum, a starch(e.g. corn starch, pregeletanized starch), a sugar (e.g., lactose,mannitol, sucrose, dextrose), a cellulosic material (e.g.microcrystalline cellulose), an acrylate (e.g, polymethylacrylate),calcium carbonate, magnesium oxide, talc, or mixtures thereof.

Oral and Parenteral Administration: In preparing the compositions inoral dosage form, any of the usual pharmaceutical media may be employed.Thus, for liquid oral preparations, such as, suspensions, elixirs, andsolutions, suitable carriers and additives include water, glycols, oils,alcohols, flavoring agents, preservatives, coloring agents, and thelike. For solid oral preparations such as, powders, capsules, andtablets, suitable carriers and additives include starches, sugars,diluents, granulating agents, lubricants, binders, disintegratingagents, and the like. Due to their ease in administration, tablets andcapsules represent the most advantageous oral dosage unit form. Ifdesired, tablets may be sugar coated or enteric coated by standardtechniques.

For parenteral formulations, the carrier will usually comprise sterilewater, though other ingredients may be included, such as ingredientsthat aid solubility or for preservation. Injectable solutions may alsobe prepared in which case appropriate stabilizing agents may beemployed.

In some applications. it may be advantageous to utilize the active agentin a “vectorized” form, such as by encapsulation of the active agent ina liposome or other encapsulant medium, or by fixation of the activeagent, e.g.. by covalent bonding, chelation, or associativecoordination, on a suitable biomolecule, such as those selected fromproteins, lipoproteins, glycoproteins, and polysaccharides.

Methods of treatment using formulations suitable for oral administrationmay be presented as discrete units such as capsules, cachets, tablets,or lozenges, each containing a predetermined amount of the activeingredient. Optionally, a suspension in an aqueous liquor or anon-aqueous liquid may be employed, such as a syrup, an elixir, anemulsion, or a draught.

A tablet may be made by compression or molding, or wet granulation,optionally with one or more accessory ingredients. Compressed tabletsmay be prepared by compressing in a suitable machine, with the activecompound being in a free-flowing form such as a powder or granules whichoptionally is mixed with, for example, a hinder, disintegrant,lubricant, inert diluent, surface active agent, or discharging agent.Molded tablets comprised of a mixture of the powdered active compoundwith a suitable carrier may be made by molding in a suitable machine.

A syrup may be made by adding the active compound to a concentratedaqueous solution of a sugar, for example sucrose, to which may also beadded any accessory ingredient(s). Such accessory ingredient(s) mayinclude flavorings, suitable preservative, agents to retardcrystallization of the sugar, and agents to increase the solubility ofany other ingredient, such as a polyhydroxy alcohol, for exampleglycerol or sorbitol.

Formulations suitable for parenteral administration may comprise asterile aqueous preparation of the active compound, which preferably isisotonic with the blood of the recipient (e.g., physiological salinesolution). Such formulations may include suspending agents andthickening agents and liposomes or other microparticulate systems whichare designed to target the compound to blood components or one or moreorgans. The formulations may be presented in unit-dose or multi-doseform.

Parenteral administration may comprise any suitable form of systemicdelivery. Administration may for example be intravenous, intra-arterial,intrathecal, intramuscular, subcutaneous, intramuscular, intra-abdominal(e.g., intraperitoneal), etc., and may be effected by infusion pumps(external or implantable) or any other suitable means appropriate to thedesired administration modality.

Nasal and other mucosal spray formulations (e.g. inhalable forms) cancomprise purified aqueous solutions of the active compounds withpreservative agents and isotonic agents. Such formulations arepreferably adjusted to a pH and isotonic state compatible with the nasalor other mucous membranes. Alternatively, they can be in the form offinely divided solid powders suspended in a gas carrier. Suchformulations may be delivered by any suitable means or method, e.g., bynebulizer, atomizer, metered dose inhaler, or the like.

Formulations for rectal administration may be presented as a suppositorywith a suitable carrier such as cocoa butter, hydrogenated fats, orhydrogenated fatty carboxylic acids.

Transdermal formulations may be prepared by incorporating the activeagent in a thixotropic or gelatinous carrier such as a cellulosicmedium, e.g., methyl cellulose or hydroxyethyl cellulose, with theresulting formulation then being packed in a transdermal device adaptedto be secured in dermal contact with the skin of a wearer.

In addition to the aforementioned ingredients, formulations of thisinvention may further include one or more ingredient selected fromdiluents, buffers, flavoring agents, binders, disintegrants, surfaceactive agents, thickeners, lubricants, preservatives (includingantioxidants), and the like.

The formulations may be of immediate release, sustained release,delayed-onset release or any other release profile known to one skilledin the art.

For administration to mammals, and particularly humans, it is expectedthat the physician will determine the actual dosage and duration oftreatment, which will be most suitable for an individual and can varywith the age, weight, genetics and/or response of the particularindividual.

The methods of the invention comprise administration of a compound at atherapeutically effective amount. The therapeutically effective amountmay include various dosages.

In one embodiment, a compound of this invention is administered at adosage of 1-3000 mg per day. In additional embodiments, a compound ofthis invention is administered at a dose of 1-10 mg per day, 3-26 mg perday, 3-60 mg per day, 3-16 mg per day, 3-30 mg per day, 10-26 mg perday, 15-60 mg, 50-100 mg per day, 50-200 mg per day, 100-250 mg per day,125-300 mg per day, 20-50 mg per day, 5-50 mg per day, 200-500 mg perday, 125-500 mg per day, 500-1000 mg per day, 200-1000 mg per day,1000-2000 mg per day, 1000-3000 mg per day, 125-3000 mg per day,2000-3000 mg per day, 300-1500 mg per day or 100-1000 mg per day. In oneembodiment, a compound of this invention is administered at a dosage of25 mg per day. In one embodiment, a compound of this invention isadministered at a dosage of 40 mg per day. In one embodiment, a compoundof this invention is administered at a dosage of 50 mg per day. In oneembodiment, a compound of this invention is administered at a dosage of67.5 mg per day. In one embodiment, a compound of this invention isadministered at a dosage of 75 mg per day. In one embodiment, a compoundof this invention is administered at a dosage of 80 mg per day. In oneembodiment, a compound of this invention is administered at a dosage of100 mg per day. In one embodiment, a compound of this invention isadministered at a dosage of 125 mg per day. In one embodiment, acompound of this invention is administered at a dosage of 250 mg perday. In one embodiment, a compound of this invention is administered ata dosage of 300 mg per day. In one embodiment, a compound of thisinvention is administered at a dosage of 500 mg per day. In oneembodiment, a compound of this invention is administered at a dosage of600 mg per day. In one embodiment, a compound of this invention isadministered at a dosage of 1000 mg per day. In one embodiment, acompound of this invention is administered at a dosage of 1500 mg perday. In one embodiment, a compound of this invention is administered ata dosage of 2000 mg per day. In one embodiment, a compound of thisinvention is administered at a dosage of 2500 mg per day. In oneembodiment, a compound of this invention is administered at a dosage of3000 mg per day.

The methods may comprise administering a compound at various dosages.For example, the compound may be administered at a dosage of 3 mg, 10mg, 30 mg, 40 mg, 50 mg, 80 mg, 100 mg, 120 mg, 125 mg, 200 mg, 250 mg,300 mg, 450 mg, 500 mg, 600 mg, 900 mg, 1000 mg, 1500 mg, 2000 mg, 2500mg or 3000 mg.

Alternatively, the compound may be administered at a dosage of 0.1mg/kg/day. The compound may administered at a dosage between 0.2 to 30mg/kg/day, or 0.2 mg/kg/day, 0.3 mg/kg/day, 1mg/kg/day, 3 mg/kg/day, 5mg/kg/day, 10 mg/kg/day, 20 mg/kg/day, 30 mg/kg/day, 50 mg/kg/day or 100mg/kg/day.

The pharmaceutical composition may be a solid dosage form, a solution,or a transdermal patch. Solid dosage forms include, but are not limitedto, tablets and capsules.

The following examples are presented in order to more fully illustratethe preferred embodiments of the invention. They should in no way,however, be construed as limiting the broad scope of the invention.

EXAMPLES Example 1 Synthesis of SARDs

Synthesis of intermediates 9-10

(2R)-1-Methacryloylpyrrolidin-2-carboxylic acid (2)

D-Proline (1, 14.93 g, 0.13 mol) was dissolved in 71 mL of 2 N NaOH andcooled in an ice bath. The resulting alkaline solution was diluted withacetone (71 mL). An acetone solution (71 mL) of methacryloyl chloride(13.56 g, 0.13 mol) and 2 N NaOH solution (71 mL) were simultaneouslyadded over 40 min to the aqueous solution of D-proline in an ice bath.The temperature of the mixture was kept at 10-11° C. during the additionof the methacryloyl chloride. After stirring (3 hours (h), roomtemperature (RT)), the mixture was evaporated in vacuo at a temperatureof 35-45° C. to remove acetone. The resulting solution was washed withethyl ether and was acidified to pH 2 with concentrated HCl. The acidicmixture was saturated with NaCl and was extracted with EtOAc (100 mL×3).The combined extracts were dried over Na₂SO₄, filtered through Collie®,and evaporated in vacuo to give the crude product as a colorless oil.Recrystallization of the oil from ethyl ether and hexanes afforded 16.2g (68%) of the desired compound as colorless crystals: mp 102.1-103.4°C. (lit. mp 102.5-103.5° C.); the NMR spectrum of this compounddemonstrated the existence of two rotamers of the title compound.

¹H NMR (300 MHz. DMSO-d₆) δ 5.28 (s) and 5.15 (s) for the first rotamer,5.15 (s) and 5.03 (s) for the second rotamer (totally 2H for bothrotamers, vinyl CH₂), 4.48-4.44 for the first rotamer, 4.24-4.20 (m) forthe second rotamer (totally 1H for both rotamers, CH at the chiralcenter), 3.57-3.38 (m, 2H, CH₂), 2.27-2.12 (IH, CH), 1.97-1.72 (m, 6H,CH₂, CH, Me); ¹³C NMR (75 MHz, DMSO-d₆) δ for major rotamer 173.3,169.1, 140.9, 116.4, 58.3, 48.7, 28.9, 24.7, 19.5: for minor rotamer174.0, 170.0, 141.6, 115.2, 60.3, 45.9, 31.0, 22.3, 19.7; IR (KBr) 3437(OH), 1737 (C═O), 1647 (CO, COOH), 1584, 1508, 1459, 1369, 1348, 1178cm⁻¹[α]_(D) ²⁶+80.8° (c=1, MeOH); Anal. Calcd. for C₉H₁₃NO₃: C 59.00, H7.15, N 7.65. Found: C 59.13, H 7.19, N7.61.

(3R,8aR)-3-Bromomethyl-3-methyl-tetrahydro-pyrrolo[2,1-c][1,4]oxazine-1,4-dione(3)

A solution of NBS (23.5 g, 0.132 mol) in 100 mL of DMF was addeddropwise to a stirred solution of the (methyl-acryloyl)-pyrrolidine(16.1 g, 88 mmol) in 70 mL of DMF under argon at RT, and the resultingmixture was stirred 3 days. The solvent was removed in vacuo, and ayellow solid was precipitated. The solid was suspended in water, stirredovernight at RT, filtered, and dried to give 18.6 g (81%) (smallerweight when dried ˜34%) of the titled compound as a yellow solid: mp158.1-160.3° C.;

¹H NMR (300 MHz. DMSO-d₆) δ 4.69 (dd, J=9.6 Hz, J=6.7 Hz, 1H, CH at thechiral center), 4.02 (d, J=11.4 Hz, 1H, CHH_(a)), 3.86 (d, J=11.4 Hz,1H, CHH_(b)), 3.53-3.24 (m, 4H, CH₂). 2.30-2.20 (m, 1H, CH), 2.04-1.72(m, 3H, CH₂ and CH), 1.56 (s, 2H, Me); ¹³C NMR (75 MHz, DMSO-d₆) δ167.3, 163.1, 83.9, 57.2, 45.4, 37.8, 29.0, 22.9, 21.6; IR (KBr) 3474,1745 (C═O), 1687 (C═O), 1448, 1377, 1360, 1308, 1227, 1159, 1062 cm⁻¹;[α]_(D) ²⁶+124.5° (c=1.3, chloroform); Anal. Calcd. for C₉H₁₂BrNO₃: C41.24, H 4.61, N 5.34. Found: C 41.46, H 4.64, N 5.32.

(2R)-3-Bromo-2-hydroxy-2-methylpropanoic acid (4)

A mixture of bromolactone (18.5 g, 71 mmol) in 300 mL of 24% HBr washeated at reflux for 1 h. The resulting solution was diluted with brine(200 mL), and was extracted with ethyl acetate (100 mL×4). The combinedextracts were washed with saturated NaHCO₃ (100 mL×4). The aqueoussolution was acidified with concentrated HCl to pH=1. which, in turn,was extracted with ethyl acetate (100 mL×4). The combined organicsolution was dried over Na₂SO₄, filtered through Celite®, and evaporatedin vacuo to dryness. Recrystallization from toluene afforded 10.2 g(86%) of the desired compound as colorless crystals: mp 110.3-113.8° C.;

¹ H NMR (300 MHz, DMSO-d₆) δ 3.63 (d, J=10.1 Hz, 1H, CHH_(a)), 3.52 (d,J=10.1 Hz, 1H, CHH_(b)), 1.35 (s, 3H, Me); IR (KBr) 3434 (OH), 3300-2500(COON), 1730 (C═O), 1449, 1421, 1380, 1292, 1193, 1085 cm⁻¹; [α]_(D)²⁶+10.5° (c=2.6, MeOH); Anal. Calcd. for C₄H₇BrO₃; C 26.25, H 3.86.Found: C 26.28. H 3.75.

(2R)-3-Bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide(8)

Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooledsolution (less than 4° C.) of (R)-3-bromo-2-hydroxy-2-methylpropanoicacid (4, 51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere.The resulting mixture was stirred for 3 h under the same condition. Tothis was added Et₃N (39.14 g, 0.39 mol) and stirred for 20 min under thesame condition. After 20 min, 5-amino-2-cyanobenzotrifluoride (6, 40.0g, 0.21 mol), 400 mL of THF were added and then the mixture was allowedto stir overnight at RT. The solvent was removed under reduced pressureto give a solid which was treated with 300 mL of H₂O, and extracted withEtOAc (2×400 mL). The combined organic extracts were washed withsaturated NaHCO₃ solution (2×300 mL) and brine (300 mL). The organiclayer was dried over MgSO₄ and concentrated under reduced pressure togive a solid which was purified from column chromatography usingCH₂C1₂/EtOAc (80:20) to give a solid. This solid was recrystallized fromCH₂Cl₂/hexane to give 55.8 g (73.9%) of(2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamideas a light-yellow solid. ¹H NMR (CDCl_(3/)TMS) δ 1.66 (s, 3H, CH₃), 3.11(s, 1H, OH), 3.63 (d, J=10.8 Hz, 1H, CH₂), 4.05 (d, J=10.8 Hz, 1H, CH₂),7.85 (d, J=8.4 Hz, 1H, ArH), 7.99 (dd, J=2.1, 8.4 Hz, 1H, ArH), 8.12 (d,J=2.1 Hz, 1H, ArH), 9.04 (bs, 1H, NH). MS (ESI) 349.0 [M−H]⁻; mp124-126° C.

(2R)-3-Bromo-N-(4-cyano-3-chlorophenyl)-2-hydroxy-2-methylpropanamide(7)

Under an argon atmosphere, thionyl chloride (15 mL, 0.20 mol) was addeddropwise to a cooled solution (less than 4° C.) of(R)-3-bromo-2-hydroxy-2-methylpropanoic acid (4, 24.3 g, 0.133 mol) in300 mL of THF at ice-water bath. The resulting mixture stirred for 3 hunder the same condition. To this was added Et₃N (35 mL, 0.245 mol) andstirred for 20 min under the same condition. After 20 min, a solution of4-amino-2-chlorobenzonitrile (5, 15.6 g, 0.10 mol) in 100 mL of THF wereadded and then the mixture was allowed to stir overnight at RT. Thesolvent removed under reduced pressure to give a solid. which treatedwith 300 mL of H₂O, and extracted with EtOAc (2×150 mL). The combinedorganic extracts washed with saturated NaHCO₃ solution (2×150 mL) andbrine (300 mL). The organic layer was dried over MgSO₄ and concentratedunder reduced pressure to give a solid, which purified by flash columnchromatography using CH₂Cl₂/EtOAc (80:20) to give a solid. This solidwas recrystallized from CH₂Cl₂/hexane to give 31.8 g (73%) of(2R)-3-bromo-N-(4-cyano-3-chlorophenyl)-2-hydroxy-2-methylpropanamide(7) as a light-yellow solid. ¹H NMR (CDCl3, 400 MHz) δ 1.7 (s, 3H, CH₃),3.0 (s, 1H, OH), 3.7 (d, 1H, CH), 4.0 (d, 1H, CH), 7.5 (d, 1H, ArH), 7.7(d, 1H, ArH), 8.0 (s, 1H, ArH), 8.8 (s, 1H, NH). MS: 342 (M+23); mp 129°C.

(S)-N-(3-Chloro-4-cyanophenyl)-2-methyloxirane-2-carboxamide (9)

A mixture of3-bromo-N-(4-cyano-3-chlorophenyl)-2-hydroxy-2-methylpropanamide (7,0.84 mmol) and potassium carbonate (1.68 mmol) in 10 mL acetone washeated to reflux for 30 min. After complete conversion of startingbromide 7 to desired epoxide 9 as monitored by TLC, the solvent wasevaporated under reduced pressure to give yellowish residue, which waspoured into 10 mL of anhydrous EtOAc. The solution was filtered throughCelite® pad to remove K₂CO₃ residue and condensed under reduced pressureto give epoxide 9 as a light yellowish solid.

¹H NMR (CDCl₃, 400 MHz) δ 8.41 (bs, NH), 8.02 (d, J=2.0 Hz, 1H, ArH),7.91 (dd, J=2.0, 8.4 Hz, 1H, ArH), 7.79 (d, J=2.0 Hz, 1H, ArH), 3.01 (s,2H), 1.69 (s, 3H). MS (ESI) m/z 235.0 [M−H]⁻.

5-Membered Ring Compounds

Five membered ring compounds of the invention were made using thefollowing general synthetic routes (Method A and Method B) where m=0.Variables X and Y are defined as necessary to obtain the desiredcompound.

Method A:

Preparation of lithium diisopropylamide (LDA) solution in THF: To astirred solution of freshly distilled diisopropylamine (0.14 mL, 1.2mmol) in anhydrous 5 mL of THF was added a solution of n-butyllithium(0.53 mL, 1.32 mmol, 2.5 M solution in hexane) at −78° C. under argonatmosphere. The prepared solution of LDA or commercial 2.0 M LDA wasslowly warmed to 0° C. and stirred for 10 min and cooled again to −78°C.. To the LDA solution was added dropwise a solution of 9′ (1.0 mmol)in 5 mL of THF for 20 min. Compound 7 or 8 in THF was added dropwisethrough dropping funnel under argon atmosphere at −78° C. The reactionmixture was stirred at the same temperature for 30 min and quenched byaddition of sat. NH₄Cl. The solution was concentrated under reducedpressure and dispersed into excess EtOAc and dried over Na₂SO₄. Thesolution was concentrated and the resulting solid was recrystallizedfrom EtOAc/hexane or DCM/hexane to give designed compound 10′. Themother liquor was concentrated and purified by flash columnchromatography (EtOAc/hexane) to give a second crop of 10′.

Method B:

The steps through the synthesis of the oxiranes 9 and 10 are the same asabove for Scheme 1. NaH of 60% dispersion in mineral oil (228 mg, 5.7mmol) was added in 20 mL of anhydrous THF solvent into a 100 mL driedtwo necked round bottom flask equipped with a dropping funnel. Acompound of general structure 12′ (2.84 mmol) was added to the solutionunder argon atmosphere in ice-water bath, and the resulting solution wasstirred for 30 min at the ice-water bath. Into the flask. epoxide 9 or10 (2.84 mmol in THF) was added through dropping funnel under argonatmosphere at the ice-water bath and stirred overnight at RT. Afteradding 1 mL of H₂O, the reaction mixture was condensed under reducedpressure, and then dispersed into 50 mL of EtOAc. washed with 50 mL (×2)water, brine, dried over anhydrous MgSO₄, and evaporated to dryness. Themixture was purified with flash column chromatography with an eluent ofEtOAc/ hexane, and the condensed compounds were then recrystallized inEtOAc/hexane to give a product of general structure 13′.

The synthetic procedure for 1001 as an example:

(S)-3-(3-Cyano-1H-pyrrol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₇H₁₃F₃N₄O₂) (1001)

To a solution of 1H-pyrrole-3-carbonitrile (0.10 g, 0.00108 mol) inanhydrous THF (10 mL). which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.090g, 0.00217 mol). After addition. the resulting mixture was stirred for 3h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 0.38 g, 0.00108 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using ethyl acetate and hexanes (1:1) as eluent to afford 0.26 gof the titled compound as pinkish solid.

Compound 1001 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.44 (s, 1H, NH), 8.44 (s, 1H, ArH), 8.24 (d, J=8.8 Hz, 1H, ArH), 8.10(d, J=8.8 Hz, 1H, ArH), 7.49 (s, 1H, Pyrrole-H), 6.38 (t, J=2.0 Hz, 1H,Pyrrole-H), 6.41-6.40 (m 2H, OH and Pyrrole-H), 4.30 (d, J=14.0 Hz, 1H,CH), 4.14 (d, J=14.0 Hz, 1H, CH), 1.34 (s, 3H, CH₃); (ESI, Positive):363.1079[M+H]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₂F₄N₄O₂) (1002)

To a solution of 4-fluoro-pyrazole (0.10 g, 0.00116 mol) in anhydrousTHF (10 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.12 g,0.00291 mol). After addition, the resulting mixture was stirred for 3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8) (0.41 g, 0.00116 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using ethyl acetate and hexanes (1:1) as eluent toafford 0.13 g of the titled compound as white solid.

Compound 1002 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.39 (s, 1H, NH), 8.47 (d, J=1.6 Hz, 1H, ArH), 8.24 (dd, J=8.4 Hz,J=2.0 Hz, 1H, ArH), 8.10 (d, J=8.4 Hz, 1H, ArH), 7.73 (d, J=4.4 Hz, 1H,Pyrazole-H), 7.41 (d, J=4.4 Hz, 1H, Pyrazole-H), 6.31 (s, 1H, OH), 4.38(d, J=14.0 Hz, 1H, CH), 4.21 (d, J=14.0 Hz, 1H, CH), 1.34 (s, 3H, CH₃);Mass (ESI, Positive): 357.0966[M+H]⁺; mp 109-111° C.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide hydrochloride (C15H₁₃ClF₄N₄O₂)(1002-HCl)

To a solution of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(0.100 g, 0.2807 mmol) in 3 mL of methanol was added hydrochloride (2 MHCl in ether, 0.15 mL. 0.2947 mol). After addition, the resultingmixture was stirred for 1-2 h at RT. Solvent was removed under vacuum,and dried to afford 0.11 g (99%) of the titled compound as white foam.

to(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamideoxalate (C₁₇H₁₄F₄N₄O₆) (1002-oxalic acid salt)

To a solution of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(0.050 g, 0.14034 mmol) in 2 mL of methanol was added oxalic acid(0.0177 g, 0.14034 mol). After addition, the resulting mixture wasstirred for 1-2 h at RT. Diethyl ether was added to above solution, andthe solid was filtered, and dried under vacuum to afford 0.058 g (92%)of the titled compound as white solid.

Compound 1002-oxalate was characterized as follows: ¹H NMR (400 MHz,DMSO-d₆) δ 14.02 (bs, 2H), 10.38 (s, 1H, NH), 8.46 (s, 1H, ArH), 8.24(d, J=8.4 Hz, 1H, ArH), 8.10 (d, J=8.4 Hz, 1H, ArH), 7.73 (d, J=4.8 Hz,1H, Pyrazole-H), 7.41 (d, J=4.0 Hz, 1H, Pyrazole-H), 6.30 (s, 1H, OH),4.38 (d, J=14.0 Hz, 1H, CH), 4.31 (s, 2H), 4.21 (d, J=14.0 Hz, 1H, CH),2.42 (s, 4H), 1.34 (s, 3H, CH₃).

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide2.3-dihydroxysuccinate (C₁₉H₁₈F₄N₄O₈) (1002-tartaric acid salt)

To a solution of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(0.050 g, 0.14034 mmol) in 2 mL of methanol was added L-(+)-tartaricacid (0.021 g, 0.14034 mol). After addition, the resulting mixture wasstirred for 1-2 h at RT. Diethyl ether was added to above solution, andthe solid was filtered and dried under vacuum to afford 0.067 g (94%) ofthe titled compound as white solid. Compound 1002- tartaric acid saltwas characterized as follows: ¹ H NMR (400 MHz, DMSO-d₆) δ 12.69 (s,2H), 10.38 (s, 1H, NH), 8.46 (s, 1H, ArH), 8.24 (d, J=8.4 Hz, 1H, ArH),8.10 (d, J=8.4 Hz, 1H, ArH), 7.73 (d, J=4.4 Hz, 1H, Pyrazole-H), 7.41(d, J=4.0 Hz, 1H, Pyrazole-H), 6.30 (s, 1H, OH), 5.08 (s, 2H, OH), 4.38(d, J=14.0 Hz, 1H, CH), 4.31 (s, 2H), 4.21 (d, J=14.0 Hz, 1H, CH), 2.42(s, 4H), 1.34 (s, 3H, CH₃).

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamidehydrobromide (C₁₅H₁₃BrF₄N₄O₂) (1002-HBr)

To a solution of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(0.050 g, 0.1403 mmol) in 2 mL of methanol was added hydrobromide (48%w/w aqueous solution, 0.0159 mL, 0.1403 mol). After addition, theresulting mixture was stirred for 1-2 h at RT. Solvent was removed undervacuum, and dried to afford 0.061 g (99%) of the titled compound asyellowish foam.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamidesuccinate (1002-succinic acid salt) (C₁₉₁-H₁₈F₄N₄O₆)

To a solution of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(0.050 g, 0.14034 mmol) in 2 mL of methanol was added succinic acid(0.0166 g, 0.14034 mol). After addition, the resulting mixture wasstirred for 1-2 h at RT. Diethyl ether was added to above solution, andthe solid was filtered and dried under vacuum to afford 0.063 g (95%) ofthe titled compound as white solid. Compound 1002- tartaric acid saltwas characterized as follows: ¹H NMR (400 MHz. DMSO-d₆) δ 12.14 (s, 2H),10.39 (s, 1H, NH), 8.46 (s, 1H, ArH), 8.24 (d, J=8.8 Hz, 1H, ArH), 8.10(d, J=8.8 Hz, 1H, ArH), 7.73 (d, J=4.4 Hz, 1H, Pyrazole-H), 7.41 (d,J=4.4 Hz, 1H, Pyrazole-H), 6.30 (s, 1H, OH), 4.39 (d, J=14.0 Hz, 1H,CH), 4.21 (d, J=14.0 Hz, 1H, CH), 2.42 (s, 4H), 1.34 (s, 3H, CH₃).

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(4-phenyl-1H-pyrazol-1-yl)propanamide(C₂₁H₁₇F₃N₄O₂) (1003)

To a solution of 4-phenyl-pyrazole (0.50 g, 0.003468 mol) in anhydrousTHF (10 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil (0.35 g,0.00867 mol). After addition. the resulting mixture was stirred for 3 h.(10-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 1.22 g, 0.003468 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using ethyl acetate and hexanes (1:2) as eluent to afford 0.90 gof the titled compound as white needles.

Compound 1003 was characterized as follows: ¹H NMR (400 MHz. DMSO-d₆) δ10.40 (s, 1H, NH), 8.46 (d, J=2.0 Hz, 1H, ArH), 8.24 (dd, J=8.4 Hz,J=2.0 Hz, 1H, ArH), 8.09 (d, J=8.4 Hz, 1H, ArH), 8.05 (s, 1H,Pyrazole-H), 7.82 (s, 1H, Pyrazole-H), 7.52-7.45 (m, 2H, ArH), 7.35-7.31(m, 2H, ArH), 7.20-7.16 (m, 1H, ArH), 6.33 (s, 1H, OH), 4.50 (d, J=14.0Hz, 1H, CH), 4.30 (d, J=14.0 Hz, 1H, CH), 1.40 (s, 3H, CH₃); Mass (ESI,Positive): 415.1455[M+H]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(3-phenyl-1H-pyrrol-1-yl)propanamide(C₂₂H₁₈F₃N₃O₂) (1004)

To a solution of 3-phenyl-pyrrole (0.50 g, 0.00349 mol) in anhydrous THF(10 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.35 g,0.00873 mol). After addition, the resulting mixture was stirred for 3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 1.23 g, 0.00349 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using ethyl acetate and hexanes (1:2) as eluent to afford 0.90 gof the titled compound as pink solid.

Compound 1004 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.41 (s, 1H, NH), 8.24 (d, J=1.6 Hz, 1H, ArH), 8.17 (dd, J=8.4 Hz,J=2.0 Hz, 1H, ArH), 8.07 (d, J=8.4 Hz, 1H, ArH), 7.38-7.33 (m, 4H, ArH),7.28-7.24 (m, 1H, ArH), 6.96 (t, J=3.0 Hz, 1H, Pyrrole-H), 6.28 (s, 1H,OH), 6.07 (t, J=3.5 Hz, 1H, Pyrrole-H), 6.03 (m, 1H, Pyrrole-H),4.30-4.22 (m, 2H, CH₂), 1.01 (s, 3H, CH₃); Mass (ESI, Positive):414.1432[M+H]⁺.

Bromo-1H-imidazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamides(1005 and 1006)

Lithium diisopropylamide solution (2.0 M) in THF/heptane/ethylbenzene (1mL) was slowly added to a solution of 4-bromo-1H-imidazole (1.0 mmol, 2mmol) in 5 mL of anhydrous THF at −78° C. and warmed to 0° C. andstirred for 10 min and cooled again to −78° C. To the solution was addeddropwise a solution of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-methyloxirane-2-carboxamide(10, 1 mmol) prepared from 8 (1 mmol) and the reaction mixture wasstirred for overnight. After quenching by addition of sat. NH₄Cl, thesolution was concentrated under reduced pressure and dispersed intoexcess EtOAc and dried over Na₂SO₄. The solution was concentrated andpurified by flash column chromatography (EtOAc/hexane) to give thedesired products as total yield of 69% (37% for 1005 and 32% for 1006)as white solids.

The compounds were characterized as follows:

(S)-3-(5-Bromo-1H-imidazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₂BrF₃N₄O₂) (1005)

Method A (using bromoamide 8 and 4-bromo-1H-imidazole instead of generalstructure 9′) gave a white solid; ¹H NMR (acetone-d₆, 400 MHz) δ 9.93(bs, 1H, NH), 8.44 (d, J=2.0 Hz, 1H), 8.26 (dd, J=8.6, 2.0 Hz, 1H), 8.03(d, J=8.6 Hz, 1H), 7.47 (s, 1H), 7.11 (s, 1H), 5.83 (s, 1H, OH), 4.50(d, J=14.0 Hz, 1H), 4.23 (d, J=14.0 Hz, 1H), 1.55 (s, 3H); ¹⁹F NMR(acetone-d₆, 400 MHz) δ 114.69; MS (ESI): 415.0[M−H]⁻; LCMS (ESI) m/zcalcd for C₁₅H₁₁N₄O₂F₃Br: 415.0088. Found: 415.0017[M−H]⁻.

(S)-3-(4-Bromo-1H-imidazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₂BrF₃N₄O₂) (1006)

Method A (using bromoamide 8 and 4-bromo- H-imidazole instead of generalstructure 9′) gave a white solid; ¹H NMR (CDCl₃, 400 MHz) δ 9.48 (bs,1H, NH), 8.15 (s, 1H), 7.97 (d, J=8.6 Hz, 1H), 7.83 (d, J=8.6 Hz, 1H),7.71 (s, 1H), 6.75 (s, 1H), 4.53 (d, J=14.4 Hz, 1H), 4.09 (d, J=14.4 Hz,1H), 2.84 (s, 1H, OH), 1.45 (s, 3H); ¹⁹F NMR (CDCl₃, 400 MHz) δ −62.19;MS (ESI): 415.0[M−H]⁻.

(S)-N-(3-Chloro-4-cyanophenyl)-2-hydroxy-3-(1H-imidazol-1-yl)-2-methylpropanamide(C₁₄H₁₃ClN₄O₂) (1008)

Method A (using bromoamide 7 and 1H-imidazole instead of generalstructure 9′) gave a yellowish solid. Yield 53%; ¹H NMR (DMSO-d₆, 400MHz) δ 10.24 (bs, 1H, NH), 8.19 (s, 1H), 7.90 (m, 2H), 7.53 (s, 1H),7.05 (s, 1H), 6.83 (s, 1H), 6.40 (bs, 1H, OH), 4.31 (d, J=14.4 Hz, 1H),4.11 (d, J=14.4 Hz, 1H), 1.34 (s, 3H); LCMS (ESI) m/z calcd forC₁₄H₁₄ClN₄O₂: 305.0805. Found: 305.0809[M+H]⁺.

(S)-N-(3-Chloro-4-cyanophenyl)-2-hydroxy-2-methyl-3-(pyrrolidin-1-yl)propanamide(C₁₅H₁₈ClN₃O₂) (1009)

Method A (using bromoamide 7 and pyrrolidine instead of generalstructure 9′) gave a yield of 89%; ¹H NMR (CDCl₃, 400 MHz) δ 9.41 (bs,1H, NH), 7.98 (d, J=2.0 Hz, 1H), 7.62 (d, J=8.8 Hz, 1H), 7.51 (dd,J=8.8, 2.0 Hz, 1H), 5.20 (s, 1H), 3.15 (d, J=12.4 Hz, 1H), 2.72 (d,J=12.4 Hz. 1H), 2.64-2.58 (m, 4H), 1.76 (m, 4H), 1.41 (s, 3H); ¹³C NMR(CDCl₃, 100 MHz) δ 175.6 (—NHCO—), 142.5, 137.9, 134.6, 119.9, 117.3,116.1, 108.0, 72.9, 62.3, 54.6 (2C). 25.5, 24.0; LCMS (ESI) m/z calcdfor C₁₅H₁₉ClN₃O₂: 308.1166. Found: 308.1173 [M+H]⁺.

Preparation of HCl salt type of(S)-N-(3-chloro-4-cyanophenyl)-2-hydroxy-2-methyl-3-(pyrrolidin-1-yl)propanamide

To a solution of 1009 in EtOH (20 mL) was added dropwise acetyl chloride(1 mL) at 0° C. and further stirred at RT overnight and removed thesolvent to gain target salt of 1009.

(S)-N-(3-Chloro-4-cyanophenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₄H₁₂ClFN₄O₂) (1007)

Method B (using oxirane 9 and 4-fluoro-1H-pyrazole instead of generalstructure 12′) gave a yellowish solid; yield 72%; ¹H NMR (CDCl₃, 400MHz) δ 8.97 (bs, 1H, NH), 7.88 (d, J=2.0 Hz, H), 7.60 (d, J=8.4 Hz, 1H),7.45 (dd, J=8.4. 2.0 Hz, 1H), 7.36 (d, J=4.0 Hz, 1H), 7.35 (d, J=4.4 Hz,1H), 5.86 (bs, 1H, OH), 4.54 (d, J=14.0 Hz, 1H), 4.15 (d, J=14.0 Hz,1H), 1.46 (s, 3H); ¹⁹F NMR (CDCl₃, 400 MHz) 5 -176.47; LCMS (ESI) m/zcalcd for C₁₄H₁₃ClFN₄O₂: 323.0711. Found: 323.0710[M+H]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3(3-(4-fluorophenyl)-1H-pyrrol-1-yl)-2-hydroxy-2-methylpropanamide(C₂₂H₁₇F₄N₃O₂) (1010)

To a solution of 3-(4-fluorophenyl)-pyrrole (0.50 g, 0.003102 mol) inanhydrous THF (10 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.37g, 0.009306 mol). After addition, the resulting mixture was stirred for3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8) (1.09 g, 0.003102 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using ethyl acetate and hexanes (1:2 to 1:1) as eluentto afford 0.60 g (45%) of the compound as yellowish solid.

Compound 1010 was characterized as follows: ¹H NMR (400 MHz, DMSO-dr) δ10.40 (s, 1H, NH), 8.42 (d, J=2.0 Hz, 1H, ArH), 8.24 (dd, J=8.8 Hz, J=2.0 Hz, 1H, ArH), 8.07 (d, J=8.8 Hz, 1H, ArH), 7.43-7.38 (m, 2H, ArH),7.11-7.05 (m, 3H, ArH), 6.73 (1, J=2.0 Hz, 1H, Pyrrole-H), 6.33 (s, 1H,OH), 4.24 (d, J=14.0 Hz, 1H, CH), 4.05 (d, J=14.0 Hz, 1H, CH), 1.37 (s,3H, CH₃); Mass (ESI, Positive): 432.1352[M+H]⁺; mp 187-189° C.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(3-phenyl-1H-pyrazol-1-yl)propanamide(C₂₁H₁₇F₃N₄O₂) (1011)

To a solution of 3-phenyl-pyrazole (0.50 g, 0.003468 mol) in anhydrousTHF (10 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.35 g,0.00867 mol). After addition. the resulting mixture was stirred for 3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 1.22 g, 0.003468 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using ethyl acetate and hexanes (1:3 to 1:2) as eluent to afford0.60 g of the titled compound as white needles.

Compound 1011 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.33 (s, 1H, NH), 8.48 (d, J=2.0 Hz, 1H, ArH), 8.22 (dd, J=8.2 Hz,J=2.0 Hz, 1H, ArH), 8.05 (d, J=8.2 Hz, 1H, ArH), 7.69 (d, J=2.0 Hz, 1H,ArH), 7.60-7.57 (m, 2H, ArH), 7.28-7.21 (m, 3H, ArH), 6.66 (d, J=3.0 Hz,1H, ArH), 6.31 (s, 1H, OH), 4.52 (d, J=14.6 Hz, 1H, CH), 4.32 (d, J=14.6Hz, 1H, CH), 1.43 (s, 3H, CH₃).

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(3-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide (C₁₅H₁₂F₄N₄O₂)(1012)

To a solution of 3-fluoro-pyrazole (0.20 g, 0.00232 mol) in anhydrousTHF (10 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.24 g,0.00582 mol). After addition, the resulting mixture was stirred for 3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8. 0.82 g, 0.00232 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄. filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using ethyl acetate and hexanes (2:1) as eluent to afford 0.36 gof the compound as white needles.

Compound 1012 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.39 (s, 1H, NH), 8.47 (d, J=2.0 Hz, 1H, ArH), 8.24 (dd, J=8.8 Hz,J=2.0 Hz, 1H, ArH), 8.11 (d, J=8.8 Hz, 1H, ArH), 7.55 (1, J=3.0 Hz, 1H,Pyrazole-H), 6.29 (s, 1H, OH), 5.93-5.91 (m, 1H, Pyrazole-H), 4.34 (d,J=13.6 Hz, 1H, CH), 4.15 (d, J=13.6 Hz, 1H, CH), 1.36 (s, 3H, CH₃); Mass(ESI, Positive): 357.0966[M+H]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(1H-pyrazol-1-yl)propanamide(C₁₅H₁₃F₃N₄O₂) (1013)

To a solution of 1H-pyrazole (0.20 g, 0.002938 mol) in anhydrous THF (10mL), which was cooled in an ice water bath under an argon atmosphere,was added sodium hydride (60% dispersion in oil, 0.29 g, 0.007344 mol).After addition, the resulting mixture was stirred for 3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 1.03 g, 0.002938 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using ethyl acetate and hexanes (2:1) as eluent to afford 0.52 gof the compound as white solid.

Compound 1013 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.39 (s, 1H, NH), 8.48 (d, J=2.0 Hz, 1H, ArH), 8.22 (dd, J=8.2 Hz,J=2.0 Hz, 1H, ArH), 8.08 (d, J=8.2 Hz, 1H, ArH), 7.66-7.65 (n, 1H,Pyrazole-H), 7.39-7.38 (m, 1H, Pyrazole-H), 6.28 (s, 1H, OH), 6.25-6.23(m, 1H, Pyrazole-H), 4.50 (d, J=13.6 Hz, 1H, CH), 4.29 (d, J=13.6 Hz,1H, CH), 1.35 (s, 3H, CH₃); Mass (ESI, Positive): 339.1105[M+H]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(3-(trifluoromethyl)-1H-pyrazol-1-yl)propanamide(C₁₆H₁₂F₆N₄O₂) (1014)

To a solution of 3-trifluoromethyl-pyrazole (0.20 g, 0.00147 mol) inanhydrous THF (10 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.15g, 0.003674 mol). After addition, the resulting mixture was stirred for3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8) (0.516 g, 0.00147 mol) was added to above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using ethyl acetate and hexanes (2:1) as eluent toafford the titled compound (103 mg, 70%) as a white solid.

Compound 1014 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.31 (bs, 1H, NH), 8.42 (d, J=2.0 Hz, 1H, ArH), 8.19 (dd, J=8.8.2.0 Hz,1H, ArH), 8,09 (d, J=8.8 Hz, 1H, ArH), 7.83 (d, J=1.2 Hz, 1H, ArH), 6.67(d, J=2.0 Hz, 1H, ArH), 6.41 (bs, OH), 4.56 (d, J=14.0 Hz, 1H, CHH),4.37 (d, J=14.0 Hz, 1H, CHH), 1.41 (s, 3H, CH₃); ¹⁹F NMR (CDCl₃,decoupling) δ −60.44, −61.25; HRMS (ESI) m/z calcd for C₁₆H₁₂F₆N₄O₂:407.0943 [M+H]⁺; Found: 407.0943 [M+H]⁺; mp 153-155° C.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(3-(4-fluorophenyl)-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₂₁H₁₆F₄N₄O₂) (1015)

To a solution of 3-(4-fluorophenyl)-pyrazole (0.30 g, 0.00185 mol) inanhydrous THF (10 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.22g, 0.00555 mol). After addition, the resulting mixture was stirred for 3h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8) (0.65 g, 0.00185 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using ethyl acetate and hexanes (2:1) as eluent to afford 0.32 g(40%) of the titled compound as pinkish solid.

Compound 1015 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.30 (s, 1H, NH), 8.41 (d, J=2.0 Hz, 1H, ArH), 8.21 (dd, J=8.2 Hz,J=2.0 Hz, 1H, ArH), 8.05 (d, J=8.2 Hz, 1H, ArH), 7.68 (d, J=2.0 Hz, 1H,ArH), 7.64-7.59 (m, 2H, ArH), 7.11-7.05 (m, 2H, ArH), 6.65 (d, J=3.0 Hz,1H, ArH), 6.31 (s, 1H, OH), 4.50 (d, J=13.6 Hz, 1H, CH), 4.30 (d,J=13.6Hz, 1H, CH), 1.42 (s, 3H, CH₃); Mass (ESI, Positive): 433.1312[M+H]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-morpholinopropanamide(C₁₆H₁₈F₃N₃O₃) (1016)

Under an argon atmosphere, 1.0 mL of lithium bis(trimethylsilyl)amide inTHF (1 mmol, Aldrich, 1 M solution in THF) was slowly added to asolution of 0.09 mL of morpholine (0.67 mmol) in THF (10 mL) at −78° C.and stiffed for 30 min at that temperature. A solution of 8 (234 mg,0.67 mmol) in 5 mL of THF was added dropwise to the solution. Thereaction mixture was stirred at the same temperature for 30 min. thenstirred overnight at RT, and quenched by an addition of sat. NH₄Clsolution. The mixture was concentrated under reduced pressure, dispersedinto excess EtOAc, dried over Na₂SO₄. concentrated and purified by flashcolumn chromatography (EtOAc/hexane) to give the target compound (209mg, yield 88%) as white solid.

Compound 1016 was characterized as follows: ¹H NMR (CDCl₃, 400 MHz) δ9.36 (bs, 1H, NH), 8.08 (d, J=1.6 Hz, 1H), 7.94 (dd, J=8.4. 1.6 Hz, 1H),7.80 (d, J=8.4 Hz, 1H), 3.68 (m, 4H), 3.28 J=13.2 Hz, 1H), 2.55 (m, 4H),2.42 (d, J=13.2 Hz, 1H), 1.50 (bs, 1H, OH), 1.42 (s, 3H); ¹⁹F NMR(acetone-d₆, 400 MHz) δ −62.20; LCMS (ES1) m/z calcd for C₁₆H₁₉F₃N₃O₃:358.1379. Found: 358.1383 [M+H]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-344-(trifluoromethyl)-1H-pyrazol-yl)propanamide(C₁₆H₁₂F₆N₄O₂) (1017)

To a solution of 4-trifluoromethyl-pyrazole (0.20 g, 0.00147 mol) inanhydrous THF (10 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.18g, 0.004409 mol). After addition, the resulting mixture was stirred for3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8) (0.516 g, 0.00147 mol) was added to above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (19:1) as eluent to afford0.30 g (50%) of the titled compound as white foam.

Compound 1017 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.38 (s, 1H, NH), 8.45 (d, J=2.0 Hz, 1H, ArH), 8.25-8.22 (m, 2H, ArH &Pyrazole-H), 8.11 (d, J=8.2 Hz, 1H, ArH), 7.82 (s, 1H, Pyrazole-H), 6.39(s, 1H, OH), 4.55 (d, J=14.0 Hz, 1H, CH), 4.37 (d, J=14.0 Hz, 1H, CH),1.40 (s, 3H, CH₃); Mass (ESI, Positive): 407.0945 [M+H]⁺.

Triazoles 1018 and 1019:

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(1H-1,2,4-triazol-1-yl)propanamide(C₁₄H₁₂F₃N₅O₂) (1018)

To a dry, nitrogen-purged 50 mL round-bottom flask, epoxide (10, 270 mg,1 mmol), 1,2,4-triazole (69 mg, 1mmol) and K₂CO₃ (268 mg, 2 mmol) weredispersed into 10 mL of 2-butanone (methylethylketone (MEK)). Themixture was heated to reflux for 12 h. The resulting mixture was cooleddown to RT. The volume of mixture was reduced under reduced pressure,poured into water, and extracted with ethyl acetate (3 times). Theorganic layer was dried over MgSO₄, concentrated and purified by flashcolumn chromatography (ethyl acetate/hexane 2:3 v/v) on silica gel toproduce target product (143 mg, 43% yield). Compound 1018 wascharacterized as follows: ¹H NMR (CDCl₃, 400 MHz) δ 9.10 (bs, 1H, NH),8.15 (s, 1H), 8.02 (d, J=2.0 Hz, 1H), 7.88 (dd, J=8.4, 2.0 Hz, 1H), 7.78(d, J=8.4 Hz, 1H), 5.70 (bs, 1H, OH), 4.79 (d, J=14.0 Hz, 1H), 4.35 (d,J=14.0 Hz, 1H), 1.53 (s, 3H); ¹⁹F NMR (CDCl₃, 400 MHz) δ −62.22; HRMS(ESI) m/z calcd for C₁₄H₁₂F₃N₅O₂ Exact Mass: 340.1021 [M+H]⁺. Found:340.1067 [M+H]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(3-(trifluoromethyl)-1H-1,2.4-triazol-1-yl)propanamide(C₁₅H₁₁F₆N₅O₂) (1019)

To a dry, nitrogen-purged 50 mL round-bottom flask, epoxide (10, 270 mg,1 mmol). 3-(trifluoromethyl)-1H-1,2,4-triazole (137 mg, 1 mmol) andK₂CO₃ (268 mg, 2 mmol) were dispersed into 10 mL of 2-butanone(methylethylketone or MEK). The mixture was heated to reflux for 12 h.The resulting mixture was cooled down to RT. The volume of mixture wasreduced under reduced pressure, poured into water, and extracted withethyl acetate (3 times). The organic layer was dried over MgSO₄,concentrated and purified by flash column chromatography (ethylacetate/hexane 2:3 v/v) on silica gel to produce target product (213 mg,53% yield).

Compound 1019 was characterized as follows: ¹H NMR (acetone-d₆, 400 MHz)δ 9.88 (bs, 1H, NH), 9.44 (s, 1H), 8.44 (s, 1H), 8.25 (d, J=8.4 Hz, 1H),8.04 (d, J=8.4 Hz, 1H), 4.82 (d, J=14.4 Hz, 1H), 4.61 (d, J=14.4 Hz,1H), 2.88 (bs, 1H, OH), 1.61 (s, 3H); ¹⁹F NMR (CDCl₃, 400 MHz) δ −62.26,−65.25; HRMS (ESI) m/z calcd for C₁₅H₁₁F₆N₅O₂ Exact Mass: 408.0895[M+H]⁺. Found: 408.0898 [M+H]⁺.

(R)-N-(4-Cyano-34 trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide (C₁₅H₁₂F₄N₄O₂)(1020)

To a solution of 4-fluoro-1H-pyrazole (0.1 g, 1.16 mmol) in anhydrousTHF (10 mL), which was cooled in an ice bath under an argon atmosphere,was added sodium hydride (60% dispersion in mineral oil, 0.12 g, 2.91mmol). After addition. the resulting mixture was stirred for 3 h.(S)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(S-isomer of 8 (8S)*; 0.41 g, 1.16 mmol) was added to the abovesolution, and the resulting reaction mixture was allowed to stirovernight at RT under argon atmosphere. The reaction was quenched bywater and extracted with ethyl acetate. The organic layer was washedwith brine, dried with anhydrous MgSO₄, filtered, and concentrated underreduced pressure. The mixture was purified by flash columnchromatography using ethyl acetate and hexanes (2/3, v/v) as eluent toafford the titled compound (127 mg, 71%) as white solid.

Compound 1020 was characterized as follows: ¹H NMR (400 MHz, CDCl₃) δ9.07 (bs, 1H, NH), 8.01 (d, J=2.0 Hz, 1H), 7.95 (dd, J=8.4. 2.0 Hz, 1H),7.78 (d, J=8.4 Hz, 1H), 7.38 (d, J=4.0 Hz, 1H), 7.34 (d, J=4.4 Hz, 1H),5.92 (s, OH), 4.54 (d, J=14.0 Hz, 1H), 4.16 (d, J=14.4 Hz, 1H), 1.47 (s,3H); ¹⁹F NMR (CDCl₃, decoupling) δ −62.23, −176.47; HRMS (ESI) m/z calcdfor C₁₅H₁₂F₄N₄O₂: 357.0975 [M+H]⁺; Found: 357.0984 [M+H]⁺; [α]_(D)²⁴+126.7° (c=1.0, MeOH) (compared with S-isomer: [α]_(D) ²⁴ −136.0°(c=0.5, MeOH)). *: 8S was synthesized from L-proline using the sameprocedure as for 8 (i.e., the R-isomer), as outlined in Scheme 1.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(3-fluoro-1H-pyrrol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₆H₁₃F₄N₃O₂) (1021)

To a solution of 3-fluoro-1-(triisopropylsilyl)-1H-pyrrole (1.21 g, 5mmol) in 20 mL of anhydrous THF, n-tetrabutylammonium fluoridetrihydrate in tetrahydrofuran (7.5 mL, 7.5 mmol; 1M) was added at RTunder argon atmosphere. The solution was stirred for 1 h. Withoutwork-up procedure, the flask was cooled down to 0° C. at ice-water bath.To the solution, NaH of 60% in mineral oil (133 mg, 3.33 mmol) wasadded. The reaction mixture was stirred for 30 min and epoxide 10 (450mg, 1.67 mmol) in anhydrous THF was added through dropping funnel underargon atmosphere at the ice-water bath and stirred overnight at RT.After quenching with 1 mL of H₂O, the reaction was condensed underreduced pressure, and then dispersed into 50 mL of EtOAc, washed withwater, evaporated, dried over anhydrous MgSO₄, and evaporated todryness. The mixture was purified with flash column chromatography byEtOAc/hexane=1/1 as eluent, and then the condensed compounds wererecrystallized with EtOAc/hexane to give a target product 1021 (181 mg,31%) as white solid.

Compound 1021 was characterized as follows: ¹H NMR (400 MHz, CDCl₃) δ8.91 (bs. 1H, NH), 8.03 ((d, J=2.0 Hz, 1H), 7.90 (dd, J=8.4, 2.0 Hz,1H), 7.81 (d, J=8.4 Hz, 1H), 6.47 (m, 1H), 6.41 (m, 1H), 5.91 (aJ=2.8.2.0 Hz, 1H), 4.36 (d, J=14.4 Hz, 1H), 3.98 (d, J=14.4 Hz, 1H),1.54 (s, 3H); ¹⁹F NMR (CDCl₃, decoupling) 8 -62.18, -164.26; HRMS (ESI)m/z. calcd for C₁₆H₁₄F₄N₃O₂: 356.1022 [M+H]⁺, Found: 356.1021 [M+H]⁺;378.0839 [H+Na]⁺.

(S)-N-(6-Cyano-5-(trifluoromethyl)pyridin-3-yl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₄H₁₁F₄N₅O₂) (1022)

(R)-3-Bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide

(R)-3-Bromo-2-hydroxy-2-methylpropanoic acid (4, 1.03 g, 0.005625 mol)reacted with thionyl chloride (0.80 g, 0.006751 mol), trimethylamine(0.74 g, 0.007313 mol), and 5-amino-3-(trifluoromethyl)picolinonitrile(1.00 g, 0.005344 mol) to afford the titled compound. The product waspurified by a silica gel column using hexanes and ethyl acetate (2:1) aseluent to afford 1.70 g (90%) of the titled compound as a yellowishsolid.

¹H NMR (400 MHz. DMSO-d₆) δ 10.82 (s, 1H, NH), 9.41 (d, J=2.0 Hz, 1H,ArH), 8.90 (d, J=2.0 Hz, 1H, ArH), 6.51 (s, 1H, OH), 3.84 (d, J=10.4 Hz,1H, CH), 3.61 (d, J=10.4 Hz, 1H, CH), 1.50 (s, 3H, CH₃); Mass (ESI,Positive): 351.9915 [M+H]⁺.

(S)-N-(6-Cyano-5-(trifluoromethyl)pyridin-3-yl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide

To a solution of 4-fluoro-pyrazole (0.20 g, 0.0023237 mol) in anhydrousTHF (5 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.28 g,0.0069711 mol). After addition, the resulting mixture was stirred for 3h.(R)-3-Bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(0.82 g, 0.0023237 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using hexanes and ethyl acetate (1:1) as eluent to afford 0.50 g(60.2%) of the titled compound as white solid.

Compound 1022 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.64 (s. 1H, NH), 9.32 (d, J=2.0 Hz, 1H, ArH), 8.82 (d, J=2.0 Hz, 1H,ArH), 7.75 (d, J=4.8 Hz, 1H, Pyrazole-H), 7.40 (d, J=4.0 Hz, 1H,Pyrazole-H), 6.41 (s, 1H, OH), 4.39 (d, J=14.0 Hz, 1H, CH), 4.22 (d,J=14.0 Hz, 1H, CH), 1.36 (s, 3H, CH₃); (ESI, Positive): 358.0939 [M+H]⁺,380.0749 [M+Na]⁺.

(S)-5-(3-(4-Fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamido)picolinamide(C₁₃H₁₄FN₅O₃) (1023)

(R)-3-Bromo-N-(6-cyanopyridin-3-yl)-2-hydroxy-2-methylpropanamide

(R)-3-Bromo-2-hydroxy-2-methylpropanoic acid (4, 3.24 g, 0.017674 mol)reacted with thionyl chloride (2.53 g, 0.021208 mol), trimethylamine(2.33 g, 0.022976 mol), and 5-aminopicolinonitrile (2.00 g, 0.01679 mol)to afford the titled compound. The product was purified by a silica gelcolumn using dichloromethane (DCM) and methanol (19:1) as eluent toafford 4.40 g (92%) of the titled compound as yellowish solid.

¹H NMR (400 MHz, DMSO-d₆) δ 10.42 (s, 1Hz, NH), 9.12 (d, J=2.4 Hz, 1H,ArH), 8.44 (dd, J=8.8 Hz, J=2.4 Hz, 1H, ArH), 8.00 (d, J=8.8 Hz, 1H,ArH), 6.40 (s, 1H, OH), 3.83 (d, J=10.4 Hz, 1H, CH), 3.59 (d, J=10.4 Hz,1H, CH), 1.49 (s, 3H, CH₃); Mass (ESI, Positive): 284.0042 [M+H]⁺.

(S)-5-(3-(4-Fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamido)picolinamide

To a solution of 4-fluoro-pyrazole (0.20 g, 0.0023237 mol) in anhydrousTHF (5 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.28 g,0.0069711 mol). After addition, the resulting mixture was stirred for 3h. (R)-3-Bromo-N-(6-cyanopyridin-3-yl)-2-hydroxy-2-methylpropanamide(0.66 g, 0.0023237 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄. filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using DCM and methanol (9:1) as eluent to afford 0.10 g (15%) ofthe titled compound as white solid.

Compound 1023 was characterized as follows: ¹H NMR (400 MHz. DMSO-d₆) δ10.08 (s, 1H, NH), 8.89 (d, J=2.4 Hz, 1H, ArH), 8.30 (dd, J=8.2 Hz,J=2.4 Hz, 1H, ArH), 8.01 (s, 1H, NH), 7.98 (d, J=8.2 Hz, 1H, ArH), 7.73(d, J=4.4 Hz, 1H, Pyrazole-H), 7.51 (s, 1H, NH), 7.42 (d, J=4.0 Hz, 1H,Pyrazole-H), 6.24 (s, 1H, OH), 4.38 (d, J=14.0 Hz, 1H, CH), 4.42 (d,J=14.0 Hz, 1H, CH), 1.34(s, 3H, CH₃); Mass (ESI, Positive): 308.1177[M+H]⁺, 330.0987 [M+Na]⁺.

N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-methylpropanamide(C₁₅H₁₂F₄N₄O) (1024)

3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-methylpropanamide

3-Bromo-2-methylpropanoic acid (2.00 g, 0.011976 mol) reacted withthionyl chloride (1.71 g, 0.014371 mol), trimethylamine (1.58 g,0.015569 mol), and 4-amino-2-(trifluoromethyl)benzonitrile (2.12 g,0.011377 mol) to afford the titled compound. The product was purified bya silica gel column using hexanes and ethyl acetate (2:1) as eluent toafford 3.50 g (91%) of the titled compound as a yellow to light brownsolid.

¹H NMR (400 MHz, DMSA-d₆) δ 10.85 (s, 1H, NH), 8.30 (s, 1H, ArH), 8.12(d, J=8.2 Hz, 1H, ArH), 8.03 (d, J=8.2 Hz, 1H, ArH), 3.72-3.67 (m, 1H,CH), 3.63-3.59 (m, 1H, CH), 3.03-2.97 (m, 1H, CH), 1.24 (d, J=6.8 Hz,3H, CH₃); Mass (ESI, Negative): 334.8.5[M−H]⁻.

N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4- fluoro-1H-pyrazol-1-yl)-2-methylpropanamide

To a solution of 4-fluoro-pyrazole (0.20 g, 0.0023237 mol) in anhydrousTHF (5 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.28 g,0.0069711 mol). After addition, the resulting mixture was stirred for 3h. 3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-methylpropanamide(0.78 g, 0.0023237 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄. filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using hexanes and ethyl acetate (1:1) as eluent to afford 0.050 gof the titled compound as yellowish solid.

Compound 1024 was characterized as follows: ¹ H NMR (400 MHz, DMSO-d₆) δ10.77 (s, 1H, NH), 8.25 (s, 1H, ArH), 8.10 (d, J=8.2 Hz, 1H, ArH), 7.96(d, J=8.2 Hz, 1H, ArH), 7.85 (d, J=4.4 Hz, 1H, Pyrazole-H), 7.47 (d,J=4.4 Hz, 1H, Pyrazole-H), 4.35-4.30 (m, 1H, CH), 4.12-4.07 (m, 1H, CH),3.12-3.10 (m, 1H, CH), 1.22 (d, J=6.8 Hz, 3H, CH₃).

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-(4-fluorophenyl)-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₂₁H₁₆F₄N₄O₂) (1025)

To a solution of 4-(4-fluorophenyl)-1H-pyrazole (0.20 g, 0.0012334 mol)in anhydrous THF (10 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.15g, 0.0037001 mol). After addition, the resulting mixture was stirred for3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.43 g, 0.0012334 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄.filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (19:1) as eluent to afford0.33 g (62%) of the titled compound as white solid.

Compound 1025 was characterized as follows: ¹ H NMR (400 MHz, DMSO-d₆) δ10.29 (s, 1H, NH), 8.41 (s, 1H, ArH), 8.21 (d, J=8.8 Hz, 1H, ArH), 8.05(d, J=8.8 Hz, 1H, ArH), 7.68 (s, 1H, Pyrazole-H), 7.61 (t, J=6.4 Hz, 2H,ArH), 7.08 (t, J=8.4 Hz. 2H, ArH), 6.65 (s, 1H, Pyrazole-H), 6.30 (s,1H, OH), 4.51 (d, J=14.0 Hz, 1H, CH), 4.31 (d, J=14.0 Hz, 1H, CH), 1.42(s, 3H, CH₃); Mass (ESI, Negative): 431.12 [M−H]⁻.

(S)-3-((1H-1,2,4-Triazol-3-yl)amino)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₄H₁₃F₃N₆O₂) (1026)

Under argon atmosphere, 100 mL round bottom flask was cooled down to 0°C. at ice-water bath. NaH of 60% in mineral oil (265 mg, 6.6 mmol) wasadded to the flask at the ice-water bath and anhydrous THF (20 mL) waspoured into the flask at that temperature. Into the flask.3-amino-1,2,4-triazole (164 mg, 2 mmol) was added into the flask at thattemperature and the reaction mixture was stirred for 30 min. Then, aprepared solution of(R)-3-bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 702 mg, 2 mmol) in anhydrous THF (10 mL) was added through droppingfunnel under argon atmosphere at the ice-water bath and stirredovernight at RT. After quenching with 1 mL of H₂O, the reaction mixturewas condensed under reduced pressure, and then dispersed into 50 mL ofEtOAc, washed with water, evaporated, dried over anhydrous MgSO₄, andevaporated to dryness. The mixture was purified with flash columnchromatography with an eluent of EtOAc/hexane (2:1 v/v) to give a targetproduct as brown solid.

Compound 1026 was characterized as follows: NMR (CDCl₃, 400 MHz) δ 9.10(bs, 1H,C(O)NH), 8.01 (m, 1H, ArH), 7.87 and 7.81 (dd, J=8.4.2.0 Hz, 1H,ArH), 7.78 (d, J=8.4 Hz, 1H, ArH), 7.72 and 7.51 (s, 1H, ArH), 5.90 and5.65 (bs, 1H, NH), 4.74 (bs, 1H, NH), 4.56 and 4.55 (d, J=14.4 and 13.6Hz, 1H, CH₂), 4.24 (bs, 1H, OH), 4.07 and 3.97 (d, J=13.6 and 14.4 Hz,1H, CH₂), 1.56 and 1.48 (s, 3H, CH); ¹⁹F NMR (acetone-d₆, 400 MHz) δ−62.24; MS (ESI) m/z 353.03 [M−H]⁻; 355.10 [M+H]⁺; HRMS (ESI) m/z, calcdfor C₁₄H₁₁F₃N₆O₂: 355.1130 [M+H]⁺, Found: 355.1128 [M+F]⁺.

tert-Butyl(S)-(1-(3-((4-cyano-3-(trifluoromethyl)phenyl)amino)-2-hydroxy-2-methyl-3-oxopropyl)-1H-pyrazol-4-yl)carbamate(C₂₀H₂₂F₃N₅O₄) (1027)

tert-Butyl-1H-pyrazol-4-ylcarbamate (1027a)

Under argon atmosphere, to a solution of IH-pyrazol-4-amine (2 g, 28.9mmol) and di-tert-butyl dicarbonate (6.3 g, 28.9 mmol) in 100 mL ofanhydrous THF was added triethylamine (1.68 mL, 12 mmol) at 0° C. Afterstirring for 30 min, the temperature was raised to RT and the mixturewas stirred for 2 h. The reaction mixture was condensed under reducedpressure, and then dispersed into 50 mL of EtOAc, washed with water,evaporated, dried over anhydrous MgSO₄, and evaporated to dryness. Themixture was purified with flash column chromatography with an eluent ofEtOAc/hexane in a 1:1 v/v ratio, and then the condensed compounds werethen recrystallized using EtOAc/hexane (1:1 v/v) to give a targetproduct. ¹H NMR (CDCl₃, 400 MHz) δ 7.63 (s, 2H, ArH), 6.29 (bs, 1H, NH),1.51 (s, 9H, C(CH₃); MS (ESI) m/z 182.1 [M−H]⁻.

(S)-tert-Butyl(1-(3-((4-cyano-3-(trifluoromethyl)phenyl)amino)-2-hydroxy-2-methyl-3-oxopropyl)-1H-pyrazol-4-yl)carbamate

Under argon atmosphere, a 100 mL round bottom flask was cooled down to0° C. at ice-water bath. NaH of 60% in mineral oil (160 mg, 4 mmol) wasadded to the flask at the ice-water bath and anhydrous THF (20 mL) waspoured into the flask at that temperature. Into the flask,tert-butyl-1H-pyrazol-4-ylcarbamate (1027a 366 mg, 2 mmol) was added atthat temperature and the reaction mixture was stirred for 30 min, then aprepared solution of(R)-3-bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 702 mg, 2 mmol) in anhydrous THF was added through a dropping funnelunder argon atmosphere at the ice-water bath and stirred overnight atRT. After quenching with 1 mL of H₂O, the reaction was condensed underreduced pressure, and then dispersed into 50 mL of EtOAc. washed withwater. evaporated, dried over anhydrous MgSO₄, and evaporated todryness. The mixture was purified with flash column chromatography usingEtOAc/hexane (2:1 v/v) as an eluent to give a target product (563 mg,62%) as yellowish solid.

Compound 1027 was characterized as follows: NMR (CDCl₃, 400 MHz) δ 9.13(bs, 1H,C(O)NH), 8.01 (d, 1H, J=8.4 Hz, ArH), 7.85 (dd, J=8.4, 1.6 Hz,1H, ArH), 7.76 (d, J=8.4 Hz, 1H, ArH), 7.63 (s, 1H, ArH), 7.43 (s, 1H,ArH), 6.21 (bs, 1H, C(O)NH), 6.17 (bs, 1H, OH), 4.54 (d, J=14.0 Hz, 1H,CH₂), 4.17 (d, J=14.0 Hz, 1H, CH₂), 1.47 (s, 9H, C(CH₃)₃), 1.45 (s,3H,CH₃); ¹⁹F NMR (acetone-d₆, 400 MHz) δ −62.10; MS (ESI) m/z 452.11[M−H]⁻; 454.06 [M+H]⁺.

(S)-3-(4-Amino-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₄F₃N₅O₂) (1028)

Under argon atmosphere, a 100 mL round bottom flask was cooled down to0° C. at ice-water bath. 5 mL of acetyl chloride was added dropwise tothe solution of 1027 (815 mg, 1.80 mmol) of anhydrous EtOH (20 mL) atthe ice-water bath. The reaction mixture was stirred for 30 min at thattemperature. The solvent was concentrated under reduced pressure, andthen dispersed into 50 mL of EtOAc, washed with water, evaporated, driedover anhydrous MgSO₄, and evaporated to dryness. The mixture waspurified with flash column chromatography EtOAc/hexane (using 3:1 to 6:1v/v ratios) as an eluent to give the target product (583 mg, 92%) asbrown solid.

Compound 1028 was characterized as follows: ¹H NMR (acetone-d₆, 400 MHz)δ 10.07 (bs, 1H,C(O)NH), 8.50 (s, 1H, ArH), 8.46 (s, 1H, ArH), 8.26 (d,J=8.0 Hz, 1H, ArH), 8.01 (d, J=8.0 Hz, 1H, ArH), 7.83 (s, 1H, ArH), 4.73(d, J=14.0 Hz, 1H, CH₂), 4.53 (d, J=14.0 Hz, 1H, CH₂), 2.95 (bs, 1H,OH), 1.51 (s, 3H, CH₃); ¹⁹F NMR (acetone-d₆, 400 MHz) δ 114.77: MS (ESI)m/z 351.98 [M−H]⁻; 354.08 [M+H]⁺.

N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)propanamide(C₁₄H₁₀F₄N₄O) (1029)

3-Bromo-N-(4-cyano-3-trifluoromethyl)phenyl)propanamide (C₁₁H₈BrF₃N₂O)

3-Bromopropanoic acid (2.00 g, 0.0130745 mol) reacted with thionylchloride (1.87 g, 0.0156894 mol), trimethylamine (1.72 g, 0.0169968mol), and 4-amino-2-(trifluoromethyl)benzonitrile (2.31 g, 0.0124207mol) to afford the titled compound. The product was purified by a silicagel column using DCM and methanol (19:1) as eluent to afford 2.31 g(55%) of the titled compound as yellowish solid. ¹H NMR (400 MHz,DMSO-d₆) δ 10.85 (s, 1H, NH), 8.28 (d, J=2.4 Hz, 1H, ArH), 8.12 (dd,J=8.8 Hz, J=2.4 Hz, 1H, ArH), 7.99 (d, J=8.8 Hz, 1H, ArH), 3.76 (t,J=6.0 Hz, 2H, CH₂), 3.06 (t, J=6.0 Hz, 2H, CH₂).

N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)propanamide(C₁₄H₁₀F₄N₄O)

To a solution of 4-fluoro-pyrazole (0.20 g, 0.0023237 mol) in anhydrousTHF (5 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.28 g,0.0069711 mol). After addition, the resulting mixture was stiffed for 3h. 3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)propanamide (1029a, 0.75g, 0.0023237 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at RT under argon. Thereaction was quenched by water, and extracted with ethyl acetate. Theorganic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using DCM and methanol (19:1) as eluent to afford 0.75 mg (10%)of the titled compound as white solid.

Compound 1029 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.81 (s, 1H, NH), 8.25 (d, J=2.4 Hz, 1H, ArH), 8.10 (dd, J=8.8 Hz,J=2.4 Hz, 1H, ArH), 7.95 (d, J=8.8 Hz, 1H, ArH), 7.88 (s, 1H,Pyrazole-H), 7.46 (s, 1H, Pyrazole-H), 4.35 (t, J=6.0 Hz, 2H, CH₂), 2.79(1, J=6.0 Hz, 2H, CH₂); Mass (ESI, Negative): 325.03 [M−H]⁻.

(S)-tert-Butyl(1-(3-((6-cyano-5-(trifluoromethyl)pyridin-3-yl)amino)-2-hydroxy-2-methyl-3-oxopropyl)-1H-pyrazol-4-yl)carbamate (C₁₉H₂₁F₃N₆O₄) (1030)

Under argon atmosphere, a 50 mL round bottom flask was cooled down to 0°C. at an ice-water bath. NaH of 60% in mineral oil (160 mg, 4 mmol) wasadded to the flask at the ice-water bath and anhydrous THF (10 mL) waspoured into the flask at that temperature.Tert-butyl-1H-pyrazol-4-ylcarbamate (1027a, 183 mg. I mmol) was addedinto the flask at that temperature and the reaction mixture was stirredfor 30 min. Then a prepared solution of(R)-3-bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(352 mg, 1 mmol) in anhydrous THF was added through dropping funnelunder argon atmosphere at the ice-water bath and stirred overnight atRT. After quenching with 1 mL of H₂O, the reaction was condensed underreduced pressure, and then dispersed into 30 mL of EtOAc, washed withwater, evaporated, dried over anhydrous MgSO₄, and evaporated todryness. The mixture was purified with flash column chromatography as aneluent EtOAc/hexane to give the target product (273 mg, 60%) asyellowish solid.

Compound 1030 was characterized as follows: ¹H NMR (CDCl₃, 400 MHz) δ9.28 (bs, 1H,C(O)NH), 8.80 (s, 1H, ArH), 8.67 (s, 1H, ArH), 7.63 (bs,1H,C(O)NH), 7.43 (s, 1H, ArH), 6.29 (bs, 1H, OH), 6.21 (s, 1H, ArH),4.55 (d, J=14.0 Hz, 1H, CH₂), 4.18 (d, J=14.0 Hz, 1H, CH₂), 1.51 (s, 3H,CH₃) 1.47 (s, 9H, C(CH₃)₃); ¹⁹F NMR (CDCl₃, 400 MHz) δ −62.11; MS (ESI)m/z 453.16 [M−H]⁻; 477.16 [M+Na]⁺.

(S)-3-(4-Acetamido-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₇H₁₆F₃N₅O₃) (1031)

Under argon atmosphere, to a solution of 1028 (150 mg, 0.43 mmol) andmethyl amine (0.09 mL, 0.64 mmol) in 10 mL of anhydrous DCM was addedacetyl chloride (AcCl, 0.038 mL, 0.53 mmol) at an ice-water bath. Afterstirring for 30 min, the temperature was raised to RT and the mixturewas stirred for 2 h. The reaction mixture was condensed under reducedpressure, and then dispersed into 10 mL of EtOAc, washed with water,evaporated, dried over anhydrous MgSO₄, and evaporated to dryness. Themixture was purified with flash column chromatography as an eluentacetone/hexane (1/2, v/v) to produce 1031 (150 mg, 89%) as white solids.

Compound 1031 was characterized as follows: ¹H NMR (CDCl₃, 400 MHz) δ9.08 (bs, 1H,C(O)NH), 7.92 (bs, 1H,C(O)NH), 7.82-7.80 (m, 2H, ArH), 7.69(d, J=8.4 Hz, 1H, ArH), 7.44 (s, 1H, ArH), 7.15 (s, 1H, ArH), 6.10 (bs,1H, OH), 4.49 (d, J=13.6 Hz, 1H, CH₂), 4.13 (d, J=13.6 Hz, 1H, CH₂),2.04 (s, 3H, NH(CO)CH₃), 1.39 (s, 3H, CH₃); ¹⁹F NMR (CDCl₃, 400 MHz) δ−62.20; MS (ESI) m/z 394.06 [M−H]⁻; 396.11[M+H]⁺.

(S)-3-(4-Amino-1H-pyrazol-1-yl)-1-((4-cyano-3-(trifluoromethyl)phenyl)amino)-2-methyl-1-oxopropan-2-yl2-chloroacetate(C₁₇H₁₅ClF₃N₅O₃) (1032); and (S)-3-(4-(2-Chloroacetamido)-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₇H₁₅ClF₃N₅O₃) (1033)

Under argon atmosphere, to a solution of 1028 (263 mg, 0.75 mmol) andtriethyl amine (0.16 mL, 1.12 mmol) in 50 mL of anhydrous DCM was addedchloroacetyl chloride (0.074 mL, 0.94 mmol) at an ice-water bath. Afterstirring for 30 min, the temperature was raised to RT and the mixturewas stirred for 2 h. The reaction mixture was condensed under reducedpressure, and then dispersed into 30 mL of EtOAc, washed with water,evaporated, dried over anhydrous MgSO₄, and evaporated to dryness. Themixture was purified with flash column chromatography as an eluentEtOAc/hexane (3/1, v/v) to produce 1032 (105 mg, 33%) and 1033 (117 mg,36%) as yellowish solids. Total yield 70%.

Compound 1032 was characterized as follows: ¹H NMR (CDCl₃, 400 MHz) δ9.22 (bs, NH₂), 8.10 (bs, 1H,C(O)NH), 7.93 (d, J=1.8 Hz, 1H, ArH), 7.86(d, J=1.8 Hz, 1H, ArH), 7.79 (d, J=8.4 Hz, 1H, ArH), 5.16 (d, J=14.8 Hz,1H, CH₂), 4.62 (d, J=14.8 Hz, 1H, CH₂), 4.11 (s, 2H, CH₂Cl), 1.77 (s,3H, CH1); ¹⁹F NMR (CDCl₃, 400 MHz) δ 114.77: MS (ESI) rniz 428.03[M−H]⁻; 452.02 [M+Na]⁺.

Compound 1033 was characterized as follows: ¹H NMR (CDCl₃, 400 MHz) δ9.12 (bs. 1H,C(O)NH), 8.12 (bs, 1H,C(O)NH), 7.99 (d, J=1.6 Hz, 1H, ArH),7.92 (s, 1H, ArH), 7.87 (dd, J=8.8, 1.6 Hz, 1H, ArH), 7.76 (d, J=8.8 Hz,1H, ArH), 7.61 (s, 1H, ArH), 6.11 (bs, 1H, OH), 4.60 (d, J=13.6 Hz, 1H,CH₂), 4.22 (d, J=13.6 Hz, 1H, CH₂), 4.17 (s, 2H, CH₂Cl), 1.47 (s, 3H,CH₃); ¹⁹F NMR (CDCl₃, 400 MHz) δ −62.19; MS (ESI) m/z 428.00 [M−H]⁻;452.01 [M+Na]⁺.

(S)-Methyl(1-(3-((4-cyano-3-(trifluoromethyl)phenyl)amino)-2-hydroxy-2-methyl-3-oxopropyl)-1H-pyrazol-4-yl)carbamate (C₁₇H₁₆F₃N₅O₄) (1034)

Under argon atmosphere, to a solution of 1028 (170 mg, 0.48 mmol) andtriethyl amine (0.16 mL, 1.15 mmol) in 10 mL of anhydrous DCM was addedmethyl carbonochloridate (0.04 mL, 0.58 mmol) at ice-water bath. Afterstirring for 30 min, the temperature was raised to RT and the mixturestirred for 2 h. The reaction mixture was condensed under reducedpressure, and then dispersed into 10 mL of EtOAc, washed with water.evaporated. dried over anhydrous MgSO₄, and evaporated to dryness. Themixture was purified with flash column chromatography as an eluentEtOAc/hexane (2/1, v/v) to produce 1034 (141 mg, 71%) as white solids.

Compound 1034 was characterized as follows: ¹H NMR (CDCl₃, 400 MHz) δ9.07 (bs, 1H,C(O)NH), 7.91 (s, 1H, ArH), 7.79 (d, J=7.2 Hz, 1H, ArH),7.69 (d, J=7.2 Hz, 1H, ArH), 7.57 (s, 1H, ArH), 7.40 (s, 1H, ArH), 6.33(bs, 1H, NH), 6.08 (bs, 1H, OH), 4.50 (d, J=13.6 Hz, 1H, CH₂), 4.12 (d,J=13.6 Hz, 1H, CH₂), 3.67 (s, 3H, NH(CO)OCH₃), 1.39 (s, 3H, CH₃); NMR(CDCl₃, 400 MHz) δ −62.21: MS (ESI) m/z 410.30[M631 H]⁻: 413.21 [M+H]⁺.

(S)-3-(4 -Acetyl-1H-pyrazol-1- yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2 - hydroxy-2-methylpropanamide(C₁₇H₁₅F₃N₄O₃) (1035)

To a solution of 1-(1H-pyrazol-4-yl)ethanone (0.10 g, 0.000908 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.11g, 0.002725 mol). After addition, the resulting mixture was stirred for3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 0.32 g, 0.000908 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (19:1) as eluent to afford70 mg (20%) of the titled compound as yellowish solid.

Compound 1035 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.37 (s, 1H, NH), 8.45 (d, J=1.2 Hz, 1H, ArH), 8.25 (s, 1H,Pyrazole-H), 8.23 (d, J=8.2 Hz, J=1.2 Hz, 1H, ArH), 8.10 (d, J=8.2 Hz,1H, ArH), 7.86 (s, 1H, Pyrazole-H), 6.37 (s, 1H, OH), 4.50 (d, J=14.0Hz, 1H, CH), 4.33 (d, J=14.0 Hz, 1H, CH), 2.34 (s, 3H, CH₃), 1.39 (s,3H, CH₃); mass (ESI, Negative): 379.14 [M−H]⁻; (ESI, Positive): 413.18[M+Na]⁺.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(4-nitro-1H-pyrazol-1-yl)propanamide(C₁₅H₁₂F₃N₅O₄) (1036)

To a solution of 4-nitro-1H-pyrazole (0.10 g, 0.0008844 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.106g, 0.002653 mol). After addition, the resulting mixture was stirred for3 h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 0.31 g, 0.0008844 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using hexanes and ethyl acetate (1:1) as eluent toafford 0.15 g (44%) of the titled compound as off-white solid.

Compound 1036 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.36 (s, 1H, NH), 8.69 (s, 1H, Pyrazole-H), 8.45 (d, J=1.2 Hz, 1H,ArH), 8.23 (d, J=8.8 Hz, J=1.2 Hz, 1H, ArH), 8.19 (s, 1H, Pyrazole-H),8.11 (d, J=8.8 Hz, 1H, ArH), 6.47 (s, 1H, OH), 4.56 (d, J=14.0 Hz, 1H,CH), 4.38 (d, J=14.0 Hz, 1H, CH), 1.41 (s, 3H, CH₃); mass (ESI,Negative): 382.13 [M−H]⁻.

(R)-3-Bromo-N-(6-cyanopyridin-3-yl)-2-hydroxy-2-methylpropanamide(C₁₀H₁₀BrN₃O₂) (1037)

(R)-3-Bromo-2-hydroxy-2-methylpropanoic acid (4, 3.24 g, 0.017674 mol)reacted with thionyl chloride (2.53 g, 0.021208 mol), trimethylamine(2.33 g, 0.022976 mol), and 5-aminopicolinonitrile (2.00 g, 0.01679 mol)to afford the titled compound. The product was purified by a silica gelcolumn using DCM and methanol (19:1) as eluent to afford 4.40 g (92%) ofthe titled compound as yellowish solid.

Compound 1037 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.42 (s, 1H, NH), 9.12 (d, J=2.4 Hz, 1H, ArH), 8.44 (dd, J=8.8 Hz,J=2.4 Hz, 1H, ArH), 8.00 (d, J=8.8 Hz, 1H, ArH), 6.40 (s, 1H, OH), 3.83(d, J=10.4 Hz, 1H, CH), 3.59 (d, J=10.4 Hz, 1H, CH), 1.49 (s, 3H, CH₃);mass (ESI, Positive): 284.0042 [M+H]⁺.

(R)-3-Bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(C₁₁H₉BrF₃N₃O₂) (1038)

(R)-3-Bromo-2-hydroxy-2-methylpropanoic acid (4, 1.03 g, 0.005625 mol)reacted with thionyl chloride (0.80 g, 0.006751 mol), trimethylamine(0.74 g, 0.007313 mol), and 5-amino-3-(trifluoromethyl)picolinonitrile(1.00 g, 0.005344 mol) to afford the titled compound. The product waspurified by a silica gel column using hexanes and ethyl acetate (2:1) aseluent to afford 1.70 g (90%) of the titled compound as yellowish solid.

Compound 1038 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.82 (s, 1H, NH), 9.41 (d, J=2.0 Hz, 1H, ArH), 8.90 (d, J=2.0 Hz, 1H,ArH), 6.51 (s, 1H, OH), 3.84 (d, J=10.4 Hz, 1H, CH), 3.61 (d, J=10.4 Hz,1H, CH), 1.50 (s, 3H, CH₃); mass (ESI, Positive): 351.9915 [M+H]⁺.

(R)-3-Bromo-2-hydroxy-2-methyl-N-(quinazolin-6-yl)propanamide(C₁₂H₁₂BrN₃O₂) (1039)

(R)-3-Bromo-2-hydroxy-2-methylpropanoic acid (2.65 g, 0.014503 mol) wasreacted with thionyl chloride (2.07 g, 0.017404 mol), trimethylamine(1.91 g, 0.018854 mol), and quinazolin-6-amine (2.00 g, 0.013778 mol) toafford the titled compound. The product was purified by a silica gelcolumn using hexanes and ethyl acetate (3:1 to 2:1) as eluent to afford0.71 g of the titled compound as yellowish solid.

Compound 1039 was characterized as follows: Mass (ESI Positive) 309.98[M+H]⁺.

3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)propanamide (C₁₁H₈BrF₃N₂O)(1040)

3-Bromopropanoic acid (2.00 g, 0.0130745 mol) reacted with thionylchloride (1.87 g, 0.0156894 mol), trimethylamine (1.72 g, 0.0169968mol), and 4-amino-2-(trifluoromethyl)benzonitrile (2.31 g, 0.0124207mol) to afford the titled compound. The product was purified by a silicagel column using DCM and methanol (19:1) as eluent to afford 2.31 g(55%) of the titled compound as yellowish solid.

Compound 1040 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.85 (s, 1H, NH), 8.28 (d, J=2.4 Hz, 1H, ArH), 8.12 (dd, J=8.8 Hz,J=2.4 Hz, 1H, ArH), 7.99 (d, J=8.8 Hz, 1H, ArH), 3.76 (t, J=6.0 Hz, 2H,CH₂), 3.06 (t, J=6.0 Hz, 2H, CH₂).

(S)—N-(2-Chloropyridin-4-yl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₂H₁₂ClFN₄O₂) (1041)

(R)-3-Bromo-N-(2-chloropyridin-4-yl)-2-hydroxy-2-methylpropanamide

Thionyl chloride (11.2 mL, 0.154 mol) was added dropwise to a cooledsolution (less than 4° C.) of (R)-3-bromo-2-hydroxy-2-methylpropanoicacid (4, 18.3 g, 0.100 mol) in 100 mL of THF under an argon atmosphere.The resulting mixture stirred for 3 h under the same condition. To thiswas added Et₃N (25.7 mL, 0.185 mol) and then stirred for 20 min underthe same condition. After 20 min, 2-chloropyridin-4-amine (9.89 g, 0.077mol), 100 mL of THF were added and then the mixture was allowed to stirovernight at RT. The solvent was removed under reduced pressure to givea solid, which was treated with 100 mL of H₂O, and extracted with EtOAc(2×50 mL). The combined organic extracts were washed with saturatedNaHCO₃ solution (2×100 mL) and brine (100 mL). The organic layer wasdried over MgSO₄ and concentrated under reduced pressure to give asolid, which was dissolved and purified by column chromatography usingCH₂Cl₂/EtOAc (80:20) to give a solid. This solid recrystallized fromCH-CH/hexane to give 12.6 g (43%) of(R)-3-bromo-N-(2-chloropyridin-4-yl)-2-hydroxy-2-methylpropanamide as alight-yellow solid. ¹H NMR (400 MHz, CDCl₃) δ 9.06 (bs, 1H, NH), 8.31(d, J=5.6 Hz, 1H), 7.77 (d, J=0.8 Hz, 1H), 7.45 (dd, J=5.6, 0.8 Hz, 1H),4.81 (bs, 1H, OH), 3.97 (d, J=10.6 Hz, 1H), 3.60 (d, J=10.6 Hz, 1H),1.64 (s, 3H); MS (ESI) m/z 295.28 [M+H]⁺.

(S)—N-(2-Chloropyridin-4-yl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₂H₁₂ClFN₄O₂)

To a dry, nitrogen-purged 100 mL round-bottom flask equipped with adropping funnel under argon atmosphere, NaH of 60% dispersion in mineraloil (96 mg, 2.4 mmol) was added in 10 mL of anhydrous THF solvent atice-water bath. 4-Fluoro-1H-pyrazole (103 mg, 1.2 mmol) was added andthe solution stirred 30 min at the ice-water bath. Into the flask, thesolution of(R)-3-bromo-N-(2-chloropyridin-4-yl)-2-hydroxy-2-methylpropanamide (293mg, 1.0 mmol) in 5 mL of anhydrous THF was added through dropping funnelunder argon atmosphere at the ice-water bath and stirred overnight atRT. After adding 1 mL of H₂O, the reaction mixture was condensed underreduced pressure, and then dispersed into 50 mL of EtOAc, washed with 50mL (×2) water, evaporated, dried over anhydrous MgSO₄, and evaporated todryness. The mixture was purified with flash column chromatography usingas an eluent EtOAc/hexane as a 1:2 ratio to produce compounds to producethe titled compound (55%) as a white solid.

Compound 1041 was characterized as follows: ¹H NMR (400 MHz, CDCl₃) δ8.90 (bs, 1H, NH), 8.26 (d, J=5.6 Hz, 1H), 7.63 (s, 1H), 7.75 (d, J=4.2Hz, 1H), 7.33 (d, J=4.2 Hz, 1H), 7.31 (dd, J=5.6, 1.2 Hz, 1H), 5.88 (s,1H, OH), 4.53 (d, J=13.6 Hz, 1H), 4.14 ((Li=13.6 Hz, 1H), 1.45 (s, 3H);¹⁹F NMR (CDCl₃, decoupled) δ −176.47; MS (ESI) m/z 298.98 [M+H]⁺; 296.96[M−H].

(S)-3-Azido-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₂H₁₀F₃N₅O₂) (1042)

A solution of 8 (351 mg, 1 mmol) in DMF (10 mL.) was treated with NaN(325 Mg, 5 mmol) under argon at 80° C. for 24 h. The reaction mixturewas then, cooled and extracted with CH₂Cl₂(3×20mL). The combined organiclayers were washed with H₂O (3×20mL) and brine, dried and evaporated togive a crude oil, which was purified by silica gel chromatography(EtOAc/n-hexane=1:2. v/v) to afford the titled compound as a yellowsolid (224 mg, 72%).

Compound 1042 was characterized as follows: ¹H NMR (400 MHz, CDCl₃) δ9.00 (bs, 1H, NH), 8.08 (s, 1H), 7.95 (d, J=8.4 Hz, 1H), 7.81 (d, J=8.4Hz, 1H), 3.92 (d, J=12.4 Hz, 1H), 3.50 (d, J=12.4 Hz, 1H), 2.96 (s, 1H,OH), 1.54 (s, 3H); ¹⁹F NMR (CDCl₃ decoupled) δ −62.21; MS (ESI) m/z314.03 [M+J]⁺; 312.18 [M−H].

(S)—N-(6-Cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methyl-3-(4-(trifluoromethyl)-1H-pyrazol-1-yl)propanamide(C₁₅H₁₁F₆N₅O₂) (1043)

To a solution of 4-trifluoromethyl-pyrazole (0.10 g, 0.0007349 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.09g, 0.002025 mol). After addition, the resulting mixture was stirred for3 h.(R)-3-Bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(0.26 g, 0.0007349 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (19:1) as eluent to afford0.18 g (60%) of the titled compound as white solid.

Compound 1043 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.63 (s. 1H, NH), 9.31 (s, 1H, ArH), 8.80 (s, 1H, ArH), 8.32 (s, 1H,Pyrazole-H), 7.81 (s, 1H, Pyrazole-H), 6.48 (s, 1H, OH), 4.55 (d, J=14.0Hz, 1H, CH), 4.37 (d, J=14.0 Hz, 1H, CH), 1.42 (s, 3H, CH₃); mass (ESI,Negative): 406.08 1M-Hr; (ESI, Positive): [M+H]⁺, 430.13 [M+Na]⁺.

(S)—N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(5-(4-fluorophenyl)-1H-1-triazol -1-yl)-2-hydroxy-2-methylpropanamide (C₂₀H₁₅F₄N₅O₂) (1044)

A mixture of 1042 (57 mg, 0.18 mmol), 1-ethylnyl-4-fluorobenzene (0.015mL, 0.18 mmol), and copper iodide (11 mg, 0.055 mmol) in AcCN/H₂O (1/0.5mL) were loaded into a vessel with a cap. The reaction vessels wereplaced in a reactor block in the microwave reactor. A programmablemicrowave (MW) irradiation cycle of 30 min on (300 W) at 100° C. and 25min off (fan-cooled) was executed twice because starting materials wereshown on TLC after the first cycle (total irradiation time, 60 min). Themixture was transferred to a round bottom flask to be concentrated underreduced pressure and poured into EtOAc, which was washed with water anddried over MgSO₄, concentrated, and purified by silica gelchromatography (EtOAc/hexane =2:1) to afford the titled compound asyellow solid (69.8 mg, 90%).

Compound 1044 was characterized as follows: ¹H NMR (400 MHz, acetone-d₆)6 9.00 (bs, 1H, NH), 8.44 (s, 1H), 8.30 (s, 1H), 8.25 (d, J=8.4 Hz, 1H),8.02 (d, J=8.4 Hz, 1H), 7.89 (dd, J=8.0, 2.4 Hz, 2H), 7.20 (d, J=8.8 Hz,2H), 5.67 (s, 1H, OH), 4.92 (d, J=14.0 Hz, 1H), 4.72 (d, J=14.0 Hz, 1H),1.60 (s, 3H); ¹⁹F NMR (acetone-d₆, decoupled) δ 114.68, 61.64; MS (ESI)m/z 432.11 [M−H]⁻434.08 [M+H]⁺. The structure of 1044 was distinguishedfrom its isomer 1045 (see below) by the 2D NMR techniques of NOESY andCOSY.

(S)—N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-(4-fluorophenyl)-1H-1,2,3-triazol-1-yl)-2-hydroxy-2-methylpropanamide(C₂₀H₁₅F₄N₅O₂) (1045)

To a suspension of copper(1)iodide (11 mg, 0.055 mmoL) in acetonitrile(7 mL)/water (3 mL) was added 1042 (57 mg, 0.182 mmol) at RT and then1-ethynyl-4-fluorobenzene (0.015 mL, 0.182 mmol) was added. Theresulting reaction mixture was stirred at RT for 3 days. The mixture wasevaporated under reduced pressure, poured into water:brine (1:1, v/v)and then extracted with ethyl acetate. The combined organic extractswere then washed with brine, dried over sodium sulfate, filtered andevaporated. Purification was by chromatography (silica, 60% ethylacetate in hexane) to afford a yellow solid (51.3 mg, 65%).

Compound 1045 was characterized as follows: ¹H NMR (400 MHz, CDCl₃) δ9.07 (bs, 1H, NH), 7.82-7.80 (m, 1H), 7.79 (s, 1H), 7.76-7.74 (m, 2H),7.72 (dd, J=8.2, 2.8 Hz, 2H), 7.10 (t, J=8.8 Hz, 2H), 5.15 (bs, 1H, OH),4.96 (d, J=14.0 Hz, 1H), 4.61 (d, J=14.0 Hz, 1H), 1.62 (s, 3H); ¹⁹F NMR(CDCl_(3,) decoupled) δ −62.24, −112.36; MS (ESI) m/z 432.17[M−H]⁻434.09 [M+H]⁺. The structure of 1045 was distinguished from itsisomer 1044 (see above) by the 2D NMR techniques of NOESY and COSY.E.g., 1045 showed an NOE cross-peak between the methylene proton and thetriazole proton indicating that these protons are within ˜4.5 Å of eachother as would be the case for 1045 but not 1044. This cross-peak wasnot seen for 1044.

(S)-3-(4-Fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methyl-N-(4-nitro-3-(trifluoromethyl)phenyl)-propanamide(C₁₄H₁₂F₄N₄O₄) (1046)

To a dry, nitrogen-purged 100 mL round-bottom flask equipped with adropping funnel under argon atmosphere containing 4-fluoro-1H-pyrazole(691 mg, 8.03 mmol), NaH of 60% dispersion in mineral oil (674 mg, 16.9mmol) was added in 60 mL of anhydrous THF solvent at ice-water bath. Themixture was stirred 30 min at the ice-water bath. Into the flask throughdropping funnel, a solution of(R)-3-bromo-2-hydroxy-2-methyl-N-(4-nitro-3-(trifluoromethyl)phenyl)propanamide(2.98 g, 8.03 mmol) in 10 mL of anhydrous THF was added under argonatmosphere at the ice-water bath, and stirred overnight at RT. Afteradding 1 mL of H₂O, the reaction mixture was condensed under reducedpressure, and then dispersed into 50 mL of EtOAc, washed with 50 mL (×2)water, evaporated, dried over anhydrous MgSO₄, and evaporated todryness. The mixture was purified with flash column chromatography usingas an eluent EtOAc/hexane in a 1:2 ratio to produce the titled compound(2.01 g, 67%) as yellow solid.

Compound 1046 was characterized as follows: ¹H NMR (400 MHz, CDCl₃) δ9.14 (bs, 1H, NH), 8.01 (s, 1H), 7.97-7.91 (m, 2H), 7.38 (d, J=3.6 Hz,1H), 7.35 (d, J=4.4 Hz, 1H), 5.95 (s, 1H, OH), 4.56 (d, J=14.0 Hz, 1H),4.17 (d, J=14.0 Hz, 1H), 1.48 (s, 3H); ¹⁹F NMR (CDCl₃, decoupled) δ−60.13, −176.47; MS (ESI) m/z 375.08 [M−H]; 377.22 [M+H]⁺; 399.04[M+Na]⁺.

(S)—N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-3-(4-iodo-1H-pyrazol-1-yl)-2-methylpropanamide(C₁₅H₁₂F₃IN₄O₂) (1047)

To a solution of 4-iodo-H-pyrazole (0.20 g, 0.001031 mol) in anhydrousTHF (5 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.124 g,0.003093 mol). After addition, the resulting mixture was stirred for 3h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 0.36 g, 0.001031 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (19:1) as eluent to afford0.25 g (52%) of the titled compound as off-white solid.

Compound 1047 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.36 (s, 1H, NH), 8.45 (s, 1H, ArH), 8.23 (d, J=8.8 Hz, J=1.2 Hz, 1H,ArH), 8.10 (d, J=8.8 Hz, 1H, ArH), 7.78 (s, 1H, Pyrazole-H), 7.46 (s,1H, Pyrazole-H), 6.31 (s, 1H, OH), 4.48 (d, J=14.0 Hz, 1H, CH), 4.31 (d,J=14.0 Hz, 1H, CH), 1.35 (s, 3H, CH₃); mass (ESI, Negative): 463.18[M−H]⁻; (ESI, Positive): 486.96 [M+Na]⁺.

(S)-3-(4-Cyano-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₆H₁₂F₃N₅O₂) (1048)

To a solution of 1H-pyrazole-4-carbonitrile (0.10 g, 0.001074 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.11g, 0.003223 mol). After addition, the resulting mixture was stirred for3h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 0.377 g, 0.001074 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using hexane and ethyl acetate (1:1 to 1:2) as eluentto afford 0.18 g (46%) of the titled compound as white solid.

Compound 1048 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.35 (s, 1H, NH), 8.45 (d, J=1.2 Hz, 1H, ArH), 8.43 (s, 1H,Pyrazole-H), 8.22 (d, J=8.8 Hz, J=1.2 Hz, H, ArH), 8.10 (d, J=8.8 Hz,1H, ArH), 7.98 (s, 1H, Pyrazole-H), 6.41 (s, 1H, OH), 4.45 (d, J=14.0Hz, 1H, CH), 4.36 (d, J=14.0 Hz, 1H, CH), 1.38 (s, 3H, CH₃); mass (ESI,Negative): 362.11 [M−H]⁻; (ESI, Positive): 386.07 [M+Na]⁺.

(S)-3-(4-Chloro-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₂ClF₃N₄O₂) (1049)

To a solution of 4-chloro-1H-pyrazole (0.15 g, 0.001463 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.18g, 0.004389 mol). After addition, the resulting mixture was stirred for3h.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(8, 0.51 g, 0.001463 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at RT underargon. The reaction was quenched by water, and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using dichloromethane and ethyl acetate (19:1) aseluent to afford 0.30 g (55%) of the titled compound as white solid.

Compound 1049 was characterized as follows: ¹H NMR (400 MHz, DMSO-d₆) δ10.38 (s, 1H, NH), 8.46 (s, 1H, ArH), 8.23 (d, J=8.6 Hz, J=1.2 Hz, 1H,ArH), 8.10 (d, J=8.6 Hz, 1H, ArH), 7.83 (s, 1H, Pyrazole-H), 7.47 (s,1H, Pyrazole-H), 6.34 (s, 1H, OH), 4.45 (d, J=14.0 Hz, 1H, CH), 4.27 (d,J=14.0 Hz, 1H, CH), 1.36 (s, 3H, CH₃); mass (ESI, Negative): 371.68[M−H]⁻.

Example 2 Octanol-Water Partition Coefficient (Log P)

Log P is the log of the octanol-water partition coefficient, commonlyused early in drug discovery efforts as a rough estimate of whether aparticular molecule is likely to cross biological membranes. Log P wascalculated using ChemDraw Ultra version is 12.0.2.1016 (Perkin-Elmer.Waltham, Massachusetts 02451). Calculated Log P values are reported inTable 1 in the column labeled ‘Log P (−0.4 to +5.6)’. Lipinski's rule offive is a set of criteria intended to predict oral bioavailability. Oneof these criteria for oral bioavailability is that the Log P is betweenthe values shown in the column heading (−0.4 (relatively hydrophilic) to+5.6 (relatively lipophilic) range), or more generally stated <5. One ofthe goals of SARD design was to improve water solubility. The monocyclictemplates of this invention such as the pyrazoles, pyrroles, etc. weremore water soluble than earlier analogs. For instance, one may comparethe Log P values of SARDs from other templates, e.g., alkyl-amine 17,indoline 100 and indole 11, to the monocyclics of the invention(1001-1064. and 1069-1071).

TABLE 1 In vitro screening of LBD binding (K_(i)), AR antagonism (IC₅₀),SARD activity, and metabolic stability wtAR Binding (K_(i)(left)) & SARDActivity (% inh): Full Transactivation (IC₅₀ (right)) Length (left) andS.V. (right) Log P (nM) Full Length S.V. DMPK (MLM) (−0.4 K_(i) (nM) %inhibition at % inhibition T_(1/2) (min) & CL_(Int) Compound # Structureto +5.6) M.W. (DHT = 1 nM IC₅₀ (nM) 1.10 μM at 10 μM (μL/min/mg)Enobosarm (agonist)

3.44 389.89  20.21 ~20 (EC₅₀) Not applicable Not applicableR-Bicalutamide

2.57 430.37 508.54 248.2  0  0 Enzalutamide

4.56 464.44 3641.29  216.3  0  0 ARN-509

3.47 477.43 1452.29   0  0  17

5.69 478.48 28.4 95   100

4.62 468.27 197.67  530.95 60 41 66.87 10.38  11

3.47 405.35 267.39  85.10 65-83 60-100 12.35 56.14 1001

2.29 362.31 327.97 partial agonist  0  0 23.5  29.5  1002

2.03 356.27 No binding  199.36 100  100  77.96  0.89 1003

3.54 414.38 No binding 1152.78  0  0 48.45 14.31 1004

3.93 413.39 322.11  178.77 (partial agonist) 0%, 40% @ 10 μM)  0  3.96175.2  1005

1.78 417.18 No binding 1019.38 50 70 16.51 41.58 1006

2.3  417.18 905.71  148.94 (partial agonist)  0  0 1007

1.66 322.72 No binding  958.77  0  0 1008

0.71 304.73 No binding 1856.8   0 30 24.61 28.16 1009

1.69 (for free amine) 307.78 (for free amine) No binding No inhibition 0  0 1010

4.09 431.38 259.29  225.91 100  60 17.93 38.66 1011

3.97 414.38 3660    4770    0  0 1012

2.49 356.27 820.97  219.48 82 73 64.07  1.02 1013

1.87 338.28 7398    1441.58  0 1014

3.21 406.28 512.3   204.59 67 (comparable to 11 in the same exp) 54(comparable to 11 in the same exp) 330    0   1015

4.13 432.37 >10000     1742   72  0 1016

1.34 357.33 1874.68  1018.68 52 80 1017

2.79 406.28 898.23  404.39 80 100  Infinity 0 1018

1.42 339.27 No binding 1091.56  0  0 1019

3.23 407.23 No binding 1012.75 68 100  1020

2.03 356.27 No binding 192   84 1021

2.41 355.39 633.23 partial  0  0 1022

1.11 357.26 No binding  92.17 54 81 1023

−0.93  307.28 No binding No effect  0 Infinity 0 1024

2.86 340.28 No binding 463.9 60 70 Infinity 0 1025

3.7  432.37 612.4  969   60  0 1026

1.19 354.29 — —  0 1027

2.24 453.41 1382.06  1153   20 1028

1.07 353.30 227.48 Agonist 1029

2.29 326.25 No Binding 2124   35 40 1030

1.32 454.40 No binding 6108   — 1031

0.78 395.34 No binding No effect — 1032

1.82 429.78 No binding  900.86 1033

1.3  411.34 No binding No effect 1034

1.3  411.34 827   1035

1.2  380.32 757.7 1036

1.9  383.28 2225     36.22 20 1037

0.7  284.11 4547    350.5 >50  1038

1.6  352.11 2490   1039

1.1  310.15 1750   1040

2.8  321.09 — 1041

0.6  298.70 2470   >75  1042

0.8  313.24 — 1043

1.8  407.27  57.91 10 1044

3.4  433.36 316.7 73 1045

3.7  433.36 250.9 84 1046

2.0  376.24 Partial 1047

3.2  464.19 1048

1.9  363.30 1049

2.4  372.73 1002-oxalic  57.99 acid salt 1002-  83.06 succinic acid salt1002-HBr  77.2 1002-tartaric 259.1 acid salt (similar to 1002 in thisexperiment) 1002-HCl 123.5 1050

2.7  417.18 >10000     427   42  0 1051

3.9  477.02 No effect 1052

3.3  482.17 5450   1053

3.4  434.35 No effect 1054

1.7  368.31 —  0  0 1055

2.3  352.31 1552    8087   1057 (Racemate)

2.0  356.27 1058

3.3  435.17 606.5  132.5 70 80 1059

4.3  450.36 600.58 285.1 70 toxic 1060

3.1  442.19 202.3  180.5 41, 23 32 1061

3.2  386.76 1345.6  331.6 41, 83 1062

2.0  376.24 Partial  1062a

— 188.16 No effect 1063

2.8  434.35 1486    216.9 1069

2.4  436.16 566.5   34.9 0, 0  0 1070

2.2  443.18 5481   90, 90 84 1071

3.0  440.38 578.5  0, 54  0

TABLE 2 MLM HLM T_(1/2) CL_(Int) T_(1/2) Compd ID Structure (min)(μL/min/mg) (min) CL_(Int) (μL/min/mg) 11

14.35 48.30 14.62 47.40 1001

23.5 29.5 1002

77.96 0.89 73.36 0.949 1004

3.96 175.2 2.261 306.5 1012

64.07 1.02

Example 3 Transactivation Assay

Methods: HEK-293 cells were transfected with the indicated receptors andGRE-LUC and CMV-renilla luc. Cells were treated 24 h after transfectionand luciferase assay performed 48 h after transfection. The SARDcompounds did not inhibit transactivation of receptors other than ARuntil 10 μM. The experimental method is described below.

Human AR was cloned into a CMV vector backbone and was used for thetransactivation study. HEK-293 cells were plated at 120,000 cells perwell of a 24 well plate in DME +5% csFBS. The cells were transfectedusing Lipofectamine (Invitrogen, Carlsbad, Calif.) with 0.25 μg GRE-LUC,0.01 μg CMV-LUC (renilla luciferase) and 25 ng of the AR. The cells weretreated 24 h after transfection and the luciferase assay performed 48 hafter transfection. Transactivation results were based on measuredluciferase light emissions and reported as relative light unit intensity(RLU). The assay was run in antagonist mode (IC₅₀) using known agonistR1881 at its EC₅₀ concentration of 0.1 nM and increasing concentrationsof SARDs of this invention. Agonist mode data was reportedqualitatively. e.g., partial agonist or an approximate EC₅₀ forenobosarm, for some compounds in Table 1. Antagonist data arerepresented as IC₅₀ (nM) obtained from four parameter logistics curveand are reported in Table 1 in the column labeled ‘IC₅₀’.

Results: Representative example graphs are shown in FIGS. 1A (1002), 2A(11 vs. 1002), 3A (1003), 4A (1004), 5A (1005), 6A (1006), 8-12(1007-1011), and 13A (1001) with results plotted as RLU reported on they-axis and SARD concentration on the x-axis (nM). In these Figures,antagonist mode data was shown as curve fitted data, whereas agonistmode data (if present) is reported without curve fitting. Only weak andpartial agonism was seen. In vivo pharmacodynamics demonstrate potentand highly efficacious antagonism of androgen dependent tissues (seeExamples 7 and 10 herein). FIG. 2 is a direct comparison of antagonismbetween 11 (closed dots) and 1002 (open dots). Other IC₅₀ valuesreported in Table 1 were calculated by the same method.

1002 was a potent antagonist (199.36 nM; Table 1 and FIG. 1A) withcomparable inhibition as 11 (85.1 nM; FIG. 2) which is an extremelypotent indole SARD lacking oral bioavailability. Despite the 2-foldincreased IC₅₀ (Table 1) and lack of AR-LSD binding (see Example 4 andTable 1). 1002 was a more potent AR degrader in vitro (see Example 5 andTable 1). Further and unlike 11, 1002 was very stable in vitro in mouse(Table 1) and human liver microsomes (Table 2) which translated intoimproved in vivo pharmacodynamics (see Example 7 herein) in mice andrats. Based on the structural differences alone, the increased SARDactivity in vitro and metabolic stability were each unexpected results.Likewise, the greatly improved in vivo efficacy could not have beenpredicted (i.e., was unexpected) based on structural differences alone.1012, 1014, and 1017 also demonstrated improved metabolic stability invitro suggesting that the pyrazole moiety may be responsible for theunexpected stability of 1002.

As discussed below, 1002 and 1014 also demonstrated significantanti-tumor activity in in vivo xenograft studies (see Examples 8 and10), suggesting that the bioavailability of these compounds issufficient for their intended uses.

1004 (pyrrole) and 1006 (imidazole) demonstrated potent inhibition(178.77 nM and 148.94 nM; Table 1; FIGS. 4A and 6A) but weak SARDactivity, whereas 1005 and 1016 demonstrated weak inhibition but strongSARD activity, suggesting that in vitro inhibition is not wellcorrelated with SARD activity. However, 1010 (pyrrole), 1012 (pyrazole),and 1014 (pyrazole) were potent inhibitors and degraders. In general,LBD binding or LBD-dependent inhibition and in vitro SARD activity seemto be separate but highly tolerant structure activity relationships.Values for other compounds of the invention are reported in Tables 1 and2.

Potent inhibition of transactivation was also seen for 1020 (192 nM),1022 (92 nM), and 1024 (464 nM). 1020 is an R-isomer of pyrazole 1002.and like 1002, does not bind to the LBD yet has strong SARD activity.Similarly, the indole SARD 11 and the R-isomer of 11 have comparableSARD activities (Table 1 and FIG. 2B) for AR-FL (LNCaP) and AR-SV(22RV1). This is in sharp contrast to propanamide SARMs such asenobosarm which typically have 100-fold lower LBD binding and agonistactivity for R-isomers (data not shown). This is further evidence thatSARD activity is not mediated through the LBD, as will be discussed inmore detail in Example 9 below. Example 9 demonstrates a novel bindingsite in the N-terminal domain (NTD), providing a basis for the distinctstructure activity relationships from traditional AR antagonists thatbind to the LBD and SARD of this invention which act through the NTD.The retention of SARD activity in opposite isomers (unlike SARMs)suggests that the NTD binding site does not require stereospecificity inits ligands. Further, the NTD binding site does not seem to require thechiral hydroxyl group which is conserved for LBD-binding (agonists and)antagonists. E.g., 1024 is a non-chiral propanamide racemate which lacksthe hydroxyl but retains SARD activity (Table 1: 60% degradation ofAR-FL) and the ability to inhibit the AR (Table 1: 1050=464 nM) despitenot binding the LBD (Table 1: K_(i): no binding). Also, 1029 replacesthe chiral center with a methylene group and yets retains some SARDactivity (Table 1: 35% degradation of AR-FL) and AR antagonism (Table 1:IC₅₀=2124 nM). 1032 has its hydroxyl group protected by acylation andand does not bind the LBD yet is an antagonist of AR. Another possibledivergence in SAR's is the A-ring which is conserved for LBD hinders as4-cyano or nitro and 3-trifluoromethyl or 3-chloro. However, changingthe CF₃ of 1002 to the Cl of 1007 ablated SARD activity. Further, 1022has a novel pyridine A-ring and docs not bind to the LBD yet retainspotent inhibition of transactivation (92 nM) and SARD activity (Table1). Similarly, SARD activity is shown for 1037 and 1041 that containpyridine A-rings (Table 1 and FIG. 28C), and 1043 is a highly potentpyridine antagonist but weak SARD activity (Table 1). Further, 1037 is a3-bromopropanamide (i.e., lacks a heterocyclic B-ring) which bindsweakly to the LBD (4547 nM) but is a potent antagonist (350.5 nM) andretains SARD activity, demonstrating that the B-ring may not benecessary (Table 1) for SARDs of this invention. Such observationsconfirm that SARD activity can be optimized in the absence of LBDbinding data and provide a rationale for the degradation of AR splicevariants lacking the LBD.

Example 4 Human Androgen Receptor (hAR) Ligand Binding Domain (LBD)Affinity Assay

Methods: hAR-LBD (633-919) was cloned into pGex4t.1. Large scaleGST-tagged AR-LBD was prepared and purified using a GST column.Recombinant AR-LBD was combined with [³H] mibolerone (PerkinElmer,Waltham, Mass.) in buffer A (10 mM Tris, pH 7.4, 1.5 mM disodium EDTA,0.25 M sucrose, 10 mM sodium molybdate, 1 mM PMSF) to determine theequilibrium dissociation constant (K_(d) of [³H]mibolerone. Protein wasincubated with increasing concentrations of [³H]mibolerone with andwithout a high concentration of unlabeled mibolerone at 4° C. for 18 hin order to determine total and non-specific binding. Non-specificbinding was then subtracted from total binding to determine specificbinding and non-linear regression for the ligand binding curve with onesite saturation was used to determine the K_(d) of mibolerone.

Increasing concentrations of SARDs or DHT (range: 10⁻¹² to 10⁻⁴ M) wereincubated with [³H]mibolerone and AR-LBD using the conditions describedabove. Following incubation, the ligand bound AR-LBD complex wasisolated using BiogeIHT hydroxyapatite, washed and counted in ascintillation counter after adding scintillation cocktail.

Results: The results of this assay are reported as KJ values (nM)inTable 1 in the column labeled ‘wt AR Binding (K_(i)(left))’. Asdiscussed above and is apparent from Table 1, there is a poorcorrelation between AR-LBD affinity and SARD activity. Eg.. see in vitroSARD activity for 1002, 1005, 1015, 1019, 1020, and 1022 despite nobinding affinity for the LBD (Table 1).

Example 5 In Vitro Assays to Determine SARD Activity

LNCaP or ADI androgen receptor degradation (full length AR): Thecompounds of the invention were tested for their effect on full lengthAR protein expression. Methods: LNCaP or ADI cells expressing fulllength AR were plated at 750,000-1,000,000 cells/well of a 6 well platein growth medium (RPMI+10% PBS). Twenty four hours after plating, themedium was changed to RPMI+1% csPBS without phenol red and maintained inthis medium for 2 days. The medium again was changed to RPMI+1% csFBSwithout phenol red and cells were treated with SARDs (1 nM to 10 mM) incombination with 0.1 nM R1881. After 24 h of treatment. cells werewashed with cold PBS and harvested. Protein was extracted usingsalt-containing lysis buffer with three freeze-thaw cycles. The proteinconcentration was estimated and five microgram of total protein wasloaded on a SDS-PAGE, fractionated, and transferred to a PVDF membrane.The membrane was probed with AR N-20 antibody (SantaCruz Biotechnology.Inc., Dallas, Tex. 75220) and actin antibody (Sigma-Aldrich, St. Louis,Mo.).

Results: Degradation in LNCaP or AD1 cells are reported in Table 1 inthe column labeled ‘Full Length % Inhibition at 1.10 μM’. The results ofthis assay were reported in FIGS. 1B (1002), 2B (11, 11R, 1002, 1020),3B-6B (1003-1006), 7 (17), 13B (1001), 20A (1010, 1012, 1014, 1015,1017, 1019 and 1022), 28A (1024 and 1029), 28C (1037 and 1041), 28D(1044 and 1045) as images of Western blot films (chemi luminescenceexposed films).

22RV1 or D567es androgen receptor degradation (splice variant (S.V.)AR): The effect of SARD treatment on the AR levels was measured inandrogen-refractory 22RV-1 or D567es prostate cancer cells. Methods:22RV1 or D567es cells expressing AR splice variants (AR-SV) were platedat 750,000-1,000,000 cells/well of a 6 well plate in growth medium(RPMI+10% FBS). Twenty four hours after plating, medium was changed andtreated. After 24-30 h of treatment, cells were washed with cold PBS andharvested. Protein was extracted using salt-containing lysis buffer withthree freeze-thaw cycles. Protein concentration was estimated and fivemicrogram of total protein was loaded on a SDS-PAGE, fractionated, andtransferred to a PVDF membrane. The membrane was probed with AR N-20antibody (Santa Cruz Biotechnology. Inc., Dallas, Tex. 75220) and actinantibody (Sigma-Aldrich, St. Louis, Mo).

Results: Degradation in 22RV1 or D567es cells are reported in Table 1 inthe column labeled “S.V. % inhibition at 10 μM.” The results of thisassay in D567es cells were reported in FIGS. 1C (1002) and 20B (1010,1012, 1014-1017, 1019 and 1022), and in 22RV1 cells in FIGS. 2B (11,11R), 13C (1001), and 28B (1024 and 1029) as images of Western blotfilms (chemiluminescence exposed films).

Example 6 Metabolism Studies with Mouse Liver Microsomes (DMPK (MLM))

Determination of Metabolic Stability (in vitro CL_(int)) of TestCompounds: Phase I Metabolism:

The assay was done in a final volume of 0.5 mL in duplicates (n=2). Thetest compound (1 mM) was pre-incubated for 10 minutes at 37° C. in 100mM Tris-HCl, pH 7.5 containing 0.5 mg/mL liver microsomal protein. Afterpre-incubation, reaction was started by addition of 1 mM NADPH(pre-incubated at 37° C.). Incubations were carried out in triplicateand at various time-points (0.5, 10, 15, 30 and 60 minutes). 100 mLaliquots were removed and quenched with 100 mL of acetonitrilecontaining internal standard. Samples were vortex mixed and centrifugedat 4000 rpm for 10 min. The supernatants were transferred to 96 wellplates and submitted for LC-MS/MS analysis. As a control, sampleincubations done in the absence of NADPH were included. From %PCR (%Parent Compound Remaining), rate of compound disappearance wasdetermined (slope) and in vitro CL_(int) (μl/min/mg protein) wascalculated.

Results: FIG. 14 reported phase 1 data as a raw data table for oneexperiment in MLM for compound 1002 and the T_(1/2) (half-life) andCL_(int) (clearance) values calculated therefrom. FIGS. 15A and 16Areport phase 1 data as a raw data table and graphed data for oneexperiment for 1002 in mouse liver microsomes (MLM) and human livermicrosomes (HLM), respectively. Similarly, FIG. 17 reported MLM data for1001 and the T_(1/2) (half-life) and CL_(int) (clearance) values inTables 1 and 2 were calculated therefrom.

Metabolic Stability in Phase I & Phase II Pathways

In this assay, the test compound was incubated with liver microsomes anddisappearance of drug was determined using discovery grade LC-MS/MS. Tosimulate Phase II metabolic pathway (glucuronidation), UDPGA andalamethicin were included in the assay. From %PCR (% Parent CompoundRemaining), rate of compound disappearance is determined (slope ofconcentration vs. time plot) and in vitro CL_(int) (μl/min/mg protein)was calculated. The results of this assay utilizing mouse livermicrosomes (MLM) are reported in Table 1 in the column labeled “DMPK(MLM) T_(1/2) (min) & CL_(int) (μL/min/mg)”. The first value is thecalculated half-life (T_(1/2)) of the test article in MLM expressed inminutes and the 2^(nd) value is the intrinsic CL (CL_(int)) of the testarticle in MLM expressed as mL/min/mg protein.

Results: FIG. 14 reported phase I & II data as a raw data table for oneexperiment and the T_(1/2) (half-life) and CL_(int) (clearance) valuescalculated therefrom. FIGS. 15B (using mouse liver microsomes (MLM)) and16B (using human liver microsomes (HLM)) reported phase I & II data for1002 as a raw data table for separate single experiments and grapheddata. This data demonstrated that 1002 is stable in MLM and very stablein HLM. The LC-MS/MS analysis was performed as described below.

The metabolic stability of 1002 and other pyrazoles of this inventionwas unexpected in view of previous SARDs (100, 17, & 11; see Table 1).See also Examples 8 and 10 for comparisons of pyrazoles to previous SARDtemplates and their unexpected results in terms of metabolicstabilities, in vivo pharmacodynamics, in vivo serum and tumorconcentrations, and in vivo anti-tumor efficacies in advanced prostatecancer (Example 10) and triple negative breast cancer (Example 8).Further, MLM data for 1024 (Table 1), a non-hydroxy variant, and 1023, apyridine A-ring compound (non-carbonitrile), both revealed a lack ofmetabolism after incubation with MLM for 60 minutes. This demonstratesmetabolic stability of SARDs of this invention including those withpyrazole B-rings, that lack the hydroxyl group, and/or includealternative A-rings.

LC-MS/MS Analysis:

The analysis of the compounds under investigation was performed usingLC-MS/MS system consisting of Agilent 1100 HPLC with an MDS/Sciex 4000Q-Trap™ mass spectrometer. The separation was achieved using a C₁₈analytical column (Alltima™, 2.1×100 mm, 3 μm) protected by a C₁₈ guardcartridge system (SecurityGuard™ ULTRA Cartridges UHPLC for 4.6 mm IDcolumns, Phenomenex). Mobile phase was consisting of channel A (95%acetonitrile +5% water +0.1% formic acid) and channel C (95% water +5%acetonitrile +0.1% formic acid) and was delivered at a flow rate 010.4mL/min. The volume ratio of acetonitrile and water was optimized foreach of the analytes. Multiple reaction monitoring scans were made withcurtain gas, collision gas, nebulizer gas, and auxiliary gas optimizedfor each compound, and source temperature at 550° C. Molecular ions wereformed using an ion spray voltage of μ4200 V (negative mode).Declustering potential, entrance potential, collision energy, production mass, and cell exit potential were optimized for each compound.

Example 7 In Vivo Antagonism Demonstrated by SARD Compound 1002

Hershberger method: Male mice (20-25 grams body weight; n=5-7/group)were either left intact or castrated and treated as indicated in theFIG.s for 13 days. Treatment of castrated mice was initiated 3 daysafter castration. Mice were sacrificed on day 14 of treatment andseminal vesicles were removed and weighed. Seminal vesicles weights wereeither represented as is or were normalized to body weight andrepresented.

Results: 1002 significantly reduced the weight of seminal vesicles at 40mg/kg oral daily dose in intact (FIG. 18A) and 100 mg/kg in castrated(FIG. 18B). The reduction in seminal vesicles weight, which isrepresentative of androgen receptor (AR) antagonism, was more pronouncedthan that of the 20 mg/kg/day enzalutamide dose. 1002 was effective evenin castrated mice, indicating that even any residual AR activity incastrated AR-target tissues was further inhibited by the potent activityof 1002 which bodes well for the abilities of SARDs of this invention totreat ADT-treated prostate cancer patients. This suggests that eventhough some weak partial AR agonism is observed in in vitrotransactivation experiments, the predominant tone in vivo is ARantagonism. Further, in vivo activity at 40 mg/kg (40 mpk) for 1002 wasa dramatic improvement over previously tested SARDs from our laboratorywhich typically only produced in vivo effects at 100 mg/kg or moredespite comparable in vitro transcriptional inhibition potencies. Thissuggests the unexpected metabolic stability of 1002 translated intoclinically significant oral bioavailability.

The Hershberger experiments were repeated in rats since rats are knownto be more sensitive models of androgenic and anabolic activities of ARagonists and antagonists. Sprague Dawley rats (165-180 gms) body weightwere treated with vehicle, 40 mpk 1002, 60 mpk 1002, or 20 mpkenzalutamide orally. After 13 days of treatment, the rats weresacrificed and the weights of prostate, seminal vesicles, and levatorani were measured. 1002 at 40 mg/kg antagonized the weights of seminalvesicles, prostate and levator ani muscle to approximately the sameextent as 20 mg/kg enzalutamide and 60 mg/kg 1002 further suppressed theweights of each of these tissues to near castration levels (FIG. 19A).FIG. 19A shows the reductions in absolute organ weights in intact ratsand FIG. 19B represents the same data of % inhibition relative tovehicle treated control. The bottom right panel of FIG. 19B presents theeffect of castration on the weights of seminal vesicles and prostate.1002 at 60 mg/kg reduced prostate and seminal vesicles weights by 70%each compared to 90% and 85% reductions, respectively, produced bycastration (not shown). 1002 is the first SARD with sufficientbioavailability to produce in vivo AR antagonism in excess ofenzalutamide despite inferior in vitro potencies in transactivation(IC₅₀) and a lack of binding to LBD (K_(i)). 1002 possesses potent SARDdegradation activities in vitro. Correspondingly, the unexpectedlysuperior in vivo antagonism of 1002 compared to enzalutamide (the IND ofenzalutamide indicated that 100 mpk and 30 mpk had comparable in vivoefficacy, so the 20 mpk dose presumably was near E_(max) and was barelysoluble) is not explainable in terms of conventional inhibition of theAR through the LBD but rather suggests that the AR antagonism isattributable to the potent degradation of the AR which is a uniqueproperty to compounds of this invention.

Sec also Example 9 for multiple biophysical lines of evidence supportingNTD binding of 1002 and other SARDs of this invention. See also Example10 for unexpected results for 1014 in a Hershberger assay, and other invivo assays.

Example 8 In Vivo Anti-Tumor Activity Demonstrated by SARD Compound 1002in Triple Negative Breast Cancer (TNBC) Patient Derived Xenografts (PDX)

Patient specimen collection and PDX creation: Specimens from breastcancer patients were collected with patient consent under a protocolapproved by the University of Tennessee Health Science Center (UTHSC)Institutional Review Board (IRB). Briefly, specimens were collectedimmediately after surgery in RPMI medium containingpenicillin:streptomycin and Fungizone (Thermo Fischer Scientific) andtransported to the laboratory on ice. The tissues were minced finely andtreated with collagenase for 2 h. The digested tissues were washed withserum-free medium and implanted as 1 mm³ fragments subcutaneously infemale Nod Scid Gamma (NSG) mice. Two such PDX from triple-negativepatients (TNBC), HBrT-1071 and HBrT-1361. characterized as TNBC at thetime of collection, were implanted in ovariectomized mice. All animalstudies were conducted under the UTHSC Animal Care and Use Committee(ACUC) approved protocols. Female NSG mice (6-8 weeks old) purchasedfrom JAX labs (Bar Harbor, Me.) were housed as five animals per cage andwere allowed free access to water and commercial rodent chow (HarlanTeklad 22/5 rodent diet-8640). HBrT-1071 and HBrT-1361 were implanted (1mm³) under the mammary fat pad surgically under isofluorane anesthesia.Once tumor sizes reached 100-200 mm³, the animals were randomized andtreated with vehicle (polyethylene glycol-300: DMSO 85:15 ratio) or 1002(60 mg/kg/day p.o.). Tumors were measured thrice weekly using caliperand the tumor volume was calculated using the formulalength*width*width*0.5236. At the end of the experiments, animals weresacrificed, tumors were weighed and collected for further processing.Blood was collected, serum was separated, and stored in −80° C.

Results: The SARD compound 1002 was able to inhibit tumor growth in twodifferent TNBC PDX models (FIG. 21A and 21B) whereas enzalutamide failedto inhibit tumor growth (FIG. 21A). 1002 significantly inhibited thegrowth of HBrt 1071 TNBC PDX with a percent tumor growth inhibition of65%. Similarly, 1002 inhibited the tumor weight by over 50% (FIG. 21A).In contrast, tumors from enzalutamide treated animals wereindistinguishable in size from vehicle treated animals, or possibledtrended toward promoting tumor growth. 1002 significantly inhibited thegrowth of HBrt-1361 TNBC PDX with a percent tumor growth inhibition of50% and inhibited the tumor weight by over 40% (FIG. 21B). Further,analyses of the AR which was present in these tumors revealed highlevels of AR splice variants (FIG. 21A, lane labeled 1071). Thisobservation helps to rationalize why 1002. an NTD-binding SARD (seeExample 9 below for biophysical evidence of NTD binding), was able toinhibit tumor growth whereas the LBD-dependent AR antagonistenzalutamide failed. This suggests that SARDs are able to inhibit ARsplice variant dependent cancers such as TNBC and advanced prostatecancers (see Example 10), e.g. those expressing AR-V7 or other AR'slacking the LBD. Further, this is confirmation that the unexpected oralbioavailability of 1002 and other SARDs of this invention, e.g, 1014 and1010. allowed serum and tumor (see also Example 10) levels followingoral administration to be sufficient for treatment of advanced andrefractory AR-dependent cancers.

Example 9 SARDs Bind to AF-1 Region of the N-Terminal Domain (NTD) ofthe Androgen Receptor

Nuclear Magnetic Resonance (NMR): AF-1 and various fragments of AF-1were cloned in pGex4t.1 and pGex6p.1 vectors. To purify proteins, largescale Luria broth cultures were induced with 1 mM isopropylβ-D-1-thiogalactopyranoside (IPTG) when the O.D. reached 0.6 andincubated at 25° C. for 6 h. Cells were harvested and lysed in a lysisbuffer (50 mM Tris pH 7.5, 25-250 mM NaCl, DNase, protease inhibitors,glycerol, EGTA, DTT, and sucrose). Protein lysates were purified usingglutathione sepharose beads by incubating overnight at 4° C. with gentlerocking and the purified protein was eluted with elution buffer (lysisbuffer without DNase) containing 50 mM reduced glutathione. Purifiedproteins were concentrated using Amicon or GE protein concentrators. Incases where GST needed to he cleaved. PreScission Protease (GE LifeSciences) was used to cleave the GST. The proteins were further purifiedusing FPLC (GE AKTA FPLC) with gel filtration (Superdex75 10/300 GL) andion exchange (HiPrep Q FF 16/10) columns. Compounds alone or incombination with purified protein were run in ¹H NMR (Bruker 400) in atotal volume of 500 μL with 5 mM protein and 200-500 mM small molecule(made in deuterated DMSO (DMSO-d₆)) in 20 mM phosphate buffer made in100% deuterated water.

NMR data were collected using a Bruker AVANCE111400 MHz NMR spectrometer(Bruker BioSpin Co. Billerica, Mass. USA) equipped with a BBO 5 mm NMRprobe, and TopSpin 3.0 software. ¹H proton NMR and Saturation-TransferDifference (STD) experiments were acquired using standard pulsesequences in the TopSpin library. Spectral width was set to 16 ppm withH₂O peak at center. 32K time domain (TD) complex data points and 256scans were used for ¹H proton NMR and 1024 scans for STD acquisition.For STD. on- and off-resonance [signals] were collected usinginterleaved method. Irradiation frequencies for on- and off-resonancewere set at 0.8 ppm and −20 ppm, respectively. STD was acquired on asample with ligand compound alone using identical settings to make surethe STD signals originated from protein in the protein-compound complexsample. Data were collected at room temperature. Chemical shift wasreferenced according to H₂O peak at 4.70 ppm.

Results: ¹H NMR has been used in high-throughput screens to detect thebinding of small molecules less than 500 Da to large proteins greaterthan 5 Kda. As opposed to other biophysical methods, it is easier to useone dimension NMR to observe changes in line-width or line broadening asa high-throughput method to identify the binding of the molecules toproteins and then use Water ligand-observed spectroscopy (WaterLOGSY) orSaturation-Transfer Difference (STD) NMR as confirmatory methodologies.These experiments are based on the fact that NMR observables such aslinewidths and NOEs vary dramatically between small molecules and largemolecules. The decreased rotational correlation times upon binding of asmall molecule ligand to a heavy target molecule produces an atypicalheavy molecule NMR result characterized by broadening and weakening ofligand peaks in ¹H NMR and negative NOE peaks in the waterLOGSY ascompared to the free state. In the absence of any affinity, the smallmolecule NMR result is obtained (sharp peaks in ¹H NMR and positiveNOEs) even in the presence of target protein. This distinction providesthe basis for NMR screening experiments.

Using these principles, ¹H NMR was utilized to confirm the binding of1002 to the AF-1 region. 1002 (500 mM) was dissolved in deuterated DMSO(DMSO-d₆) and was incubated alone or mixed with 5 mM AF-1 and thebinding of the molecules to the protein was determined by NMR. While1002 alone exhibited sharp peaks revealing the ligand present in thefree state, 1002 in combination with AF-1 provided broad, diffused, andshorter ligand peaks revealing that 1002 has affinity for AF-1 (FIG.22). To further confirm the 1D NMR results. we performed WaterLOGSY with1002 alone or in combination with AF-1. While the 1002 alone gave aflattened positive signal, 1002 in combination with AF-1 provided anegative signal, characteristic of binding to the protein (FIG. 22).These results provide evidence that 1002 binds to AF-1 in the NTD of AR,explaining how a molecule that does not hind the LBD of AR (Table 1) caninhibit the AR in vitro and in vivo.

Steady State Fluorescence: Recombinant histidine tagged AR-NTD (aminoacids 1-559) and AR-AF1 (amino acids 141-486) were purified aspreviously described. The steady-fluorescence spectrum for the proteins(1 μM) alone or after titration with increasing concentrations of 1002(1 μM, 2 μM, 5 μM, 10 μM, 25 μM, & 50 μM) was measured after excitationat 278 nm on a Shimadzu Fluorescence spectrophotometer. Proteins werepreincubated on ice for 30 minutes with 1002. The results representthree independent experiments (n-3) measured in duplicate.

Results: The pyrazole SARD 1002 showed a dramatic increase in thefluorescence signal in the region seen for tyrosine emission (FIG. 27B,307 nm). Normally, the tyrosine signal is not seen due to energytransfer to tryptophan residues in folded/partially folded polypeptides.The increase in the tyrosine signal is similar to what is seen inunfolded/denatured AR-NTD or AR-AF1, e.g., upon addition of urea (FIG.27A). However, there is no corresponding ‘red shift’ (increase inwavelength) in the tryptophan signal (compare FIGS. 27A and 27B, in ureaμ_(max) 344 nm to 347 nm). 1002 may unfold the receptor polypeptides(resulting in tyrosine emission). but shield the tryptophan residues.

For the pyrrole SARD 1010, some evidence for quenching was observed, butthe concentration dependence was poor. However, more strikingly therewas a consistent and dramatic ‘blue shift’ (toward smaller wavelengths),which was consistent with the folded form of AR-NTD/AF (i.e. TMAOspectrum in FIG. 27C. λ_(max) 344 nm to 340 nm). On the basis of data sofar it seems 1010 may stabilize the structure of the AR polypeptides.The data with the indole SARD 36 (FIG. 27D) was similar to what was seenwith 1002, but the changes in fluorescence were weaker. In each case, aninteraction was observed between the SARD and the AR-1 or NTD. Thoughthe perturbation of fluorescence polarization (FP) was not identical,these similar results across multiple templates of SARDs suggest thatthe interaction with the N-terminus of the androgen receptor is aconserved feature for the SARDs of this invention. Further, 1002 lacksan interaction with the LBD yet retains potent AR antagonism and SARDactivity.

Example 10 Metabolic Stability of Pyrazoles such as 1014 and 1002Reveals the Therapeutic Potential of SARDs In Vivo In VitroCharacteristics:

Transactivation (IC₅₀): As reported in Table I using the method ofExample 3, 1014 is a potent inhibitor of the AR with an IC₅₀ value of205 nM which is similar to 1002 (199 nM).

LBD binding (K_(i)): As reported in Table I using the method of Example4, 1014 binds to the LBD of the AR with a K_(i) value of 512 nM. whereas1002 does not bind to the LBD. SARD As reported in Table 1 using themethods of Example 5, 1014 and 1002 are capable of potently degradingfull length and splice variant androgen receptors.

LNCaP-Enzalutamide Resistant (LNCaP-EnzR) Cells MR49F Growth Assay:Cells were plated at 10,000 cells/well in RPMI +1% csFBS without phenolred medium in 96 well plates. Cells were treated in the indicated mediumwith a dose response of the SARDs. At the end of three days, medium waschanged and the cells were re-treated. At the end of 6 days, the livecells were measured by Cell-Titer-Glo (Promega) assay.

Results: 1002 and 1014 demonstrated comparable growth inhibition of anenzalutamide resistant variation of the LNCaP (LNCaP-EnzR) cell linewhich bears the double mutant F876L/T877A, conferring resistance toenzalutamide. 1002 and 1014 both had IC₅₀ values of ˜3 μM and almostcomplete inhibition at 10 μM (FIG. 23), suggesting that either SARDcould be beneficial for enzalutamide resistant prostate cancer patientsif these levels could he achieved in the tumor. (see Table 4 below)

Liver Microsome Metabolism study:

Materials: Microsomes were purchased from Xenotech, LLC. Solution ‘A’and ‘B’ (Cat # 451220. and 451200, respectively) for NADPH regeneratingsystem (NRS) solution were obtained from Corning Life Sciences.Verapamil, genistein, UDPGA, alamethicin and magnesium chloride werepurchased from Sigma-Aldrich. Saccharolactone was obtained from SantaCruz Biotechnology.

Method: Phase I

Test compound stock solutions were prepared at 10 mM in DMSO. They werediluted to a concentration of 50 μM in 50% acetonitrile (ACN)/H₂Oresulting in a working stock solution of 100×. Liver microsomes wereutilized at a Final concentration of 1.0 mg/mL of protein. Duplicatewells were used for each time point (0, 5, 10, 30, and 60 minutes).Reactions were carried out at 37° C. in a shaking water bath, and thefinal concentration of solvent was kept constant at 0.5%. At each timepoint, 100 μL of reaction was removed and added to a sample wellcontaining 100 μL of ice-cold. 100% ACN (plus internal standard), tostop the reaction. The final volume for each reaction was 200 μL,composed of: 66 μL of 0.2 M KPO₄ buffer, (pH 7.4); 50 μL of NRSsolution; and 10 μL of microsomes (20 mg/mL stock).

The NRS is a solution of glucose-6-phosphate dehydrogenase, NADP⁺,MgCl₂, and glucose-6-phosphate, prepared per manufacturer'sinstructions. Each 5.0 mL stock of NRS solution contains 3.8 mL H₂O, 1.0mL solution “A”, and 0.2 mL solution “B”. The reaction from the positivecontrol wells (verapamil, 0.5 were stopped with ice cold acetonitrilecontaining internal standard.

Phase I and II

Reaction conditions were followed similarly as described above.Additional cofactors were also included in each reaction. UDPGA wasadded at a final concentration of 5.0 mM. Saccharolactone(β-glucuronidase inhibitor) and alamethicin (pore forming peptide) wereadded to each reaction at a final concentration of 5.0 mM and 50 μg/mL,respectively. Each 200 μL of microsomal reaction was comprised of 65 μLof 0.2 M KPO₄ (pH 7.4), 50 μL of NRS mixture. 66 μL of UDPGA (15 Mmstock); 5.0 μL of saccharolactone (200 mM stock); 0.5 μL of alamethicin(20 mg/mL); 0.6 μL of MgCl₂ (1 M stock), and 10 μL of microsomes (20mg/mL stock). The reaction from the positive control wells (genistein,2.0 μM) was stopped with ice cold acetonitrile containing internalstandard.

Samples were centrifuged at 3,000 rpm for 10 minutes to remove debrisand precipitated protein. Approximately 150 μL of supernatant wassubsequently transferred to a new sample block for analysis.

Data Analysis

For half-life determination and clearance, data was fitted usingGraphPad Prism with a non-linear regression equation, and one phaseexponential decay.

Results: 1014 was compared to other compounds, including 1002 in livermicrosome metabolism studies. Interestingly, while 1002 showed ahalf-life around 1 h in vitro. 1014 had a half-life of infinity in thesame test, i.e., after 120 min of incubation over 50% of the compoundstill remained in the reaction (Table 3). As seen in Table 3. thepyrazoles 1002, 1014, and 1022 (see also Table 1 for 1023 and 1024)demonstrated much improved in vitro metabolic stabilities compared toindole (11, 34, 36) and indoline (103) based compounds (and the pyrrole1010) (Table 3) while retaining SARD activity (Table 1). This suggestedthat significant in vivo bioavailabilities may be possible for 1002 and1014.

TABLE 3 Liver microsomes MLM / RLM t_(1/2) CL_(int) (min) (μL/min/mg)1002 77.96 0.89 1014 infinity ~0 96 54.44 12.73(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(4-(trifluoromethyl)-1H-indazol-1-yl)propanamide 1010 17.93 38.66 36 11.7758.8(S)-N-(3-Chloro-4-cyanophenyl)-3-(4-fluoro-1H-indol-1-yl)-2-hydroxy-2-methylpropanamide 34 15.50 58.87(S)-N-(3-Chloro-4-cyanophenyl)-3-(5-fluoro-6-phenyl-1H-indol-1-yl)-2-hydroxy-2-methylpropanamide 11 14.35 48.30(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl-3-(5-fluoro-1H-indol-1-ly)-2-hydroxy-2-methylpropanamide 103 15 46.72(S)-N-(3-Chloro-4-cyanophenyl)-3-(4-fluoroindolin-1-yl)-2-hydroxy-2-methylpropanamide 1022 58.06 11.94

In Viva Characteristics:

1014 drug concentrations in serum and tumor in a xenograft experiment.Nude mice implanted with 22RV1 cells subcutaneously were randomized whenthe tumors reached between 100 and 200 mm³. The mice were treated withvehicle (20:80 water:PEG-400) or 60 mg/kg/day 1014 (or indicated dosesof other SARDs) in vehicle for 21 days. At the end of 21 days, the micewere sacrificed and blood and tumors were collected for furtheranalysis. Measurement of drug concentration in animals treated with 1014demonstrated a significant accumulation of the drug in serum (20.1 μM)and tumor (35.6 (Table 4 and FIG. 24) compared to other molecules testedin parallel in the same experiment. These in vivo levels for 1014. evenin view of structurally similar pyrazoles 1002 and 1012. was unexpected.Further, these levels help to explain the efficacy in LNCaP-EnzRxenografts (see FIG. 26 and its description below). Although 22RV1tumors were not susceptible to SARDs in this particular experiment,likely due to androgen independent growth, this result suggests thatandrogen-dependent tumors, e.g.. LNCaP-EnzR, would he susceptible.Another observation from these data is that tumor concentrations were inexcess of serum concentrations, suggesting accumulation of drug in thetumor. The results are shown in Table 4 and FIG. 24.

TABLE 4 Tumor Xenograft PK Xenograft concentration Serum concentrationdose (nM) (nM) (mg/kg) At sacrifice (8 hrs) 2 hrs 8 hrs 1002 60 15,7253,560 3,620 11 100 854 365 338 1012 60 6,655 2,114 1,914 1014 60 35,6384,469 20,119 96 100 4,458 1,207 2,563 1010 100 17,683 862 4,173 103 1001,748 380 1,776 36 100 7,128 570 4,142 34 100 2,948 261 965

Hershberger assay: Intact C57BL/6 male mice (6-8 weeks old) wererandomized based on body weight and treated with various compoundsindicated in FIG. 25 for 14 days. At the end of 14 days, the mice weresacrificed and seminal vesicles were weighed. 1014 demonstrated the bestinhibition of seminal vesicles weight compared to other compounds,following by 1002. suggesting that these orally administered SARDs werepresent in levels sufficient to antagonize the AR in androgen-dependenttissues of intact animals. The indoles 34 and 36. pyrrole 1010, and thepyrazole 1012 did not exhibit strong AR antagonism in vivo in thisassay.

LNCaP-Enzalutamide-Resistant (LNCaP-EnzR) Xenograft: LNCaP-EnzR cellsMR49F in RPMI+10% FBS were mixed with Matrigel (BD Biosciences) (1:1)and injected subcutaneously in NOD SCID Gamma (NSG) mice (100 μL). Oncethe tumors reached 100-200 mm³, the animals were randomized and weretreated with vehicle (20:80 water:PEG-300) or 1014 (60 mg/kg/day) invehicle. Tumor volume was measured twice weekly. At the end of thestudy, animals were sacrificed, tumors isolated, weighed, and stored forfurther analysis. The experiment was performed twice with two differentbatches of cells and the results are shown in FIG. 26. Results: In twoseparate experiments, 1014 was able attain high efficacy tumor growthinhibition, reducing tumor volumes by approximately 60-70% compared tovehicle treated animals. These results suggest that 1014 and other SARDsof this invention administered orally were capable of therapeuticefficacy in enzalutamide resistant (i.e., advanced and refractory)prostate cancers.

Conclusion: All these results indicate that 1014 has unexpectedproperties due to its slow metabolism and tumor accumulation. Although,1014 structurally is comparable to 1002, only differing slightly in thesubstitution with a CF₃ in the third position of the pyrazole ring (vs.4-fluoro for 1002), it is extremely resistant to metabolism by livermicrosomes and thereby has significant accumulation in serum, androgendependent organs, and in tumors which is unexpected in view of otherSARDs tested and in the prior art. This allowed for unexpected in vivoefficacies following oral administration. such as pharmacodynamics(Hershberger assay demonstrated most efficacious seminal vesicles weighteffect seen with a SARD) and xenograft tumor growth inhibition(LNCaP-EnzR xenograft), that would not have been possible with ourearlier reported SARD templates such as 11, 100, and 17, or other SARDsknown in the prior art.

Example 11 SARDs Antagonize F876L

FIGS. 29A-29C illustrate that SARDs antagonized F876L AR at dosescomparable to the wildtype AR and do not have any intrinsic agonistactivity in F876L, showing their ability to overcome enzalutamideresistance. In FIGS. 29A-29C, compound 1002 was able to inhibit thetranscriptional activation of wtAR and F876L (enzalutamide resistance)and W741L (bicalutamide resistance). Enzalutamide behaved similarly,however enzalutamide acted as an agonist at higher levels of treatmentof F876L. This demonstrated the ability of SARDs to overcome antagonistswitch mechanisms of resistance which are prevalent in CPRC. Further,Example 10 shows the ability of SARDs to overcome enzalutamideresistance with regard to cellular growth and with regard to xenograftgrowth.

Example 12 Binding to AR-NTD to Degrade

FIG. 32 shows that AR NTD binding of 1002 for required for degradation.Chimeric constructs were created in which the AR and GR were cloned suchthat the entire sequence was AR or GR, or the N-terminal domain wasderived from AR but the DNA binding and ligand binding domains werederived from GR (AGG) or vice versa (GAA). Several lines of evidencesummarized below suggested either NTD binding and/or dependence upon NTDfor SARD activity. Further to that line of reasoning, the SARD 1002 wastested for its ability to degrade the AR, GR, AGG or GAA constructs as away to demonstrate that AR NTD was required in order for the SARD todegrade the protein (i.e., demonstrate NTD-dependence). Other lines ofevidence suggesting NTD-dependent SARD activity included: FIGS. 22 (NMR)and 27 (fluorescent polarization) demonstrated 1002 binding to NTD andtheir ability to degrade SV's which lack any LBD further suggested NTDbinding. Example 3 discusses potent transcriptional activity in theabsence of demonstrable LBD binding and structure-activity relationshipsof NTD binding that differ from known LBD SAR patterns. Example 8discusses the ability of 1002 to inhibit SV-driven growth (i.e., FL ARis not expressed) of TNBC xenografts with SARD 1002, suggesting NTDbinding. Consistent with this interpretation, the LBD-dependent ARantagonist enzalutamide failed to inhibit TNBC xenograft growth in thesesame TNBC xenografts.

The chimeric receptor data as provided in FIG. 32 is a strong evidencefor NTD-dependence of SARD activity. From the Western blots of FIG. 32.it is apparent that SARDs degraded AR and/or AGG (NTD is AR and rest isGR) but not GR or GAA (NTD is GR and rest is AR). This suggests that ARNTD is required for SARD activity.

Example 13(S)-3-(4-Bromo-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₂BrF₃N₄O₂) (1050)

To a solution of 4-bromo-1H-pyrazole (0.20 g, 0.0013608 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.16g, 0.0040827 mol). After addition, the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.478 g, 0.001608 mol) was added to the above solution, and theresulting reaction mixture was allowed to stir overnight at roomtemperature under argon. The reaction was quenched by water andextracted with ethyl acetate. The organic layer was washed with brine,dried with MgSO₄, filtered, and concentrated under vacuum. The productwas purified by a silica gel column using DCM and ethyl acetate (19:1)as eluent to afford 0.47 g (79.6%) of the titled compound as white foam.

¹ H NMR (400 MHz, CDCl₃) δ 9.08 (s, 1H, NH), 8.00 (d, J=2.0 Hz, 1H,ArH), 7.87 (dd, J=8.4 Hz, J=2.0 Hz, 1H, ArH), 7.79 (d, J=8.4 Hz, 1H,ArH), 7.49 (s, 1H, Pyrazole-H), 7.47 (s, 1H, Pyrazole-H), 5.92 (s, 1H,OH), 4.64 (d, J=14.0 Hz, 1H, CH), 4.24 (d, J=14.0 Hz, 1H, CH), 1.47 (s,3H, CH₃).

Mass (ESI, Negative): 371.68 [M−H]⁻; (ESI, Positive): 440.94 [M+Na]⁺.

(R)-3-Bromo-N-(4-cyano-2-iodo-5-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₂H₉BrF₃IN₂O₂) (1051)

3-Bromo-2-methyl-2-hydroxypropanoic acid (0.50 g, 0.00273224 mol) wasreacted with thionyl chloride (0.39 g, 0.0032787 mol), trimethylamine(0.36 g, 0.0035519 mol), and4-amino-5-iodo-2-(trifluoromethyl)benzonitrile (0.81 g, 0.0025956 mol)to afford the titled compound. The product was purified by a silica gelcolumn using DCM and ethyl acetate (9:1) as eluent to afford 0.80 g(64.6%) of the titled compound as a light brown solid.

¹H NMR (400 MHz, CDCl₃) δ 9.53 (s, 1 H, NH), 8.92 (s, 1H, ArH), 8.24 (s,1H, ArH), 7.26 (s, 1H, OH), 4.04 (d, J=10.4 Hz, 1 H, CH), 3.62 (d,J=10.4 Hz, 1H, CH), 1.67 (s, 3H, CH₃).

Mass (ESI Positive): 479.25[M+H]⁺.

(S)-N-(4-Cyano-2-iodo-5-(trifluoromethyl)phenyl)-3-(4-fluoro-lH-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₁F₄IN₄O₂) (1052)

To a solution of 4-fluoro-1H-pyrazole (0.09 g, 0.001048 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.15g, 0.003669 mol). After addition. the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-2-iodo-5-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.50 g, 0.001048 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using hexanes and ethyl acetate (2:1 to 1:1) as eluentto afford 0.32 g (64%) of the titled compound as a white solid.

¹H NMR (400 MHz, CDCl₃) δ 9.60 (s, 1H, NH), 8.76 (s, 1H, ArH), 8.69 (s,1H, ArH), 7.76 (d, J=4.8 Hz, 1H, Pyrazole-H), 7.36 (d, J=4.4 Hz, 1H,Pyrazole-H), 6.85 (s, 1H, OH), 4.39 (d, J=14.0 Hz, 1H, CH), 4.20 (d,J=14.0 Hz, 1H, CH), 1.41 (s, 3H, CH₃).

Mass (ESI, Negative): 481.00 [M−H]⁻;

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(5-(4-fluorophenyl)-1H-tetrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₉H₁₄F₄N₆O₂) (1053)

To a solution of 5-(4-fluorophenyl)-1H-tetrazole (0.20 g, 0.001219 mol)in anhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.17g, 0.004265 mol). After addition, the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.43 g, 0.001219 mol) was added to above solution, and the resultingreaction mixture was allowed to stir 2 days at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (9:1) as eluent to afford0.053 g (10%) of the titled compound as a yellowish solid.

¹H NMR (400 MHz, CDCl₃) δ 10.39 (s, 1H, NH), 8.44 (s, 1H, ArH), 8.26 (d,J=8.2 Hz 1H, ArH), 8.10 (d, J=8.2 Hz 1H, ArH), 7.93-7.89 (m, 2H, ArH),7.30 (t, J=8.2 Hz, 2H, ArH), 6.64 (s, 1H, OH), 5.09 (d, J=14.0 Hz, 1H,CH), 4.92 (d, J=14.0 Hz, 1H, CH), 1.55 (s, 3H, CH₃).

Mass (ESL Negative): 433.17 [M−H]⁻.

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-3-(4-methoxy-1H-pyrazol-1-yl)-2-methylpropanamide(C₁₆H₁₅F₃N₄O₃) (1054)

To a solution of 4-methoxy-1H-pyrazole (0.12 g, 0.001233 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.17g, 0.004281 mol). After addition, the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.43 g, 0.001233 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (9:1) as eluent to afford0.30 g (60%) of the titled compound as a white solid.

¹H NMR (400 MHz, DMSO-d₆) δ 10.38 (s, 1H, NH), 8.46 (d, J=2.0 Hz, 1H,ArH), 8.24 (dd, J=8.2 Hz, J=2.0 Hz, 1H, ArH), 8.10 (d, J=8.2 Hz, 1H,ArH), 7.35 (d, J=0.8 Hz, 1H, Pyrazole-H), 7.15 (d, J=0.8 Hz, 1H,Pyrazole-H), 6.25 (s, 1H, OH), 4.35 (d, J=14.0 Hz, 1H, CH), 4.18 (d,J=14.0 Hz, 1H, CH), 3.61 (s, 3H, CH₃), 1.36 (s, 3H, CH₃).

HRMS [C₁₆H₁₆F₃N₄O₃ ⁺]: calcd 369.1175. found 369.1182[M+H]⁺. Purity:99.28% (HPLC).

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methyl-3-(4-methyl-1H-pyrazol-1-yl)propanamide(C₁₆H₁₅F₃N₄O₂) (1055)

To a solution of 4-methyl-1H-pyrazole (0.10 g, 0.001218 mol) inanhydrous THF (5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.17g, 0.004263 mol). After addition, the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.428 g, 0.001218 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (19:1) as eluent to afford0.28 g (66%) of the titled compound as a white solid.

¹H NMR (400 MHz, DMSO-d₆) δ 10.38 (s, 1H, NH), 8.46 (d, J=2.0 Hz, 1H,ArH), 8.23 (dd, J=8.8 Hz, J=2.0 Hz, 1H, ArH), 8.10 (d, J=8.8 Hz, 1H,ArH), 7.41 (s, 1H, Pyrazole-H), 7.17 (s, 1H, Pyrazole-H), 6.24 (s, 1H,OH), 4.40 (d, J=14.0 Hz, 1H, CH), 4.22 (d, J=14.0 Hz, 1H, CH), 1.97 (s,3H, CH₃), 1.36 (s, 3H, CH₃).

HRMS [C₁₆H₁₆F₃N₄O₂ ⁺]: calcd 353.1225, found 353.1232[M+H]⁺. Purity:99.75% (HPLC).

N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-methyloxirane-2-carboxamide(C₁₂H₉F₃N₂O₂) (1056)

2-Methyloxirane-2-carboxylic acid (1.00 g, 0.009892 mol) was reactedwith thionyl chloride (1.41 g, 0.011871 mol), trimethylamine (1.30 g,0.01286 mol), and 4-amino-2-(trifluoromethyl)benzonitrile (1.84g,0.009892 mol) to afford the titled compound. The product was purified bya silica gel column using DCM and ethyl acetate (19:1) as eluent toafford 1.52 g (57%) of the titled compound as a yellowish solid.

¹ H NMR (400 MHz, DMSO-d₆) δ 10.54 (s, 1H, NH), 8.55 (d, J=1.6-2.0 Hz,1H, ArH), 8.32 (dd, J=8.8 Hz, J=2.0 Hz, 1H, ArH), 8.12 (d, J=8.8 Hz, 1H,ArH), 6.39 (s, 1H, OH), 3.94 (d, J=11.2 Hz, 1H, CH), 3.70 (d, J=11.2 Hz,1H, CH), 1.44 (s, 3H, CH₃).

Mass (ESI, Negative): [M−H]⁻; (ESI, Positive): [M+Na]⁺.

N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₂F₄N₄O₂) (1057)

To a solution of 4-fluoro-pyrazole (0.10 g, 0.001162 mol) in anhydrousTHF (10 mL) , which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.14 g,0.003486 mol). After addition, the resulting mixture was stirred forthree to hours.N-(4-Cyano-3-(trifluoromethyl)phenyl)-2-methyloxirane-2-carboxamide(0.31 g, 0.001162 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water. extracted with ethyl acetate.The organic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using hexanes and ethyl acetate (2:1 to 1:1) as eluent to afford0.37 g (90%) of the titled compound as a yellowish solid.

¹H NMR (400 MHz, DMSO-d₆) δ 10.38 (s, 1H, NH), 8.47 (d, J=2.0 Hz, 1H,ArH), 8.24 (dd, J=8.8 Hz, J=2.0 Hz, 1H, ArH), 8.10 (d, J=8.8 Hz, 1H,ArH), 7.74 (d, J=4.4 Hz, 1H, Pyrazole-H), 7.41 (d, J=4.0 Hz, 1H,Pyrazole-H), 6.31 (s, 1H, OH), 4.39 (d, J=14.0 Hz, 1H, CH), 4.21 (d,J=14.4 Hz, 1H, CH), 1.34 (s, 3H, CH₃).

Mass (ESI, Negative): [M−H]⁻; (ESI, Positive): [M+Na]⁺.

(S)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₂H₉F₃N₂O₂)

(S)-3-Bromo-2-hydroxy-2-methylpropanoic acid (1.00 g, 0.0054645 mol)reacted with thionyl chloride (0.78 g, 0.0065574 mol), trimethylamine(0.72 g, 0.0071038 mol), and 4-amino-2-(trifluoromethyl)benzonitrile(1.02 g, 0.0054645 mol) to afford the titled compound. The product waspurified by a silica gel column using DCM and ethyl acetate (19:1) aseluent to afford 1.75 g (90%) of the titled compound as a yellowishsolid.

Mass (ESI, Positive): 351.08 [M+Na]⁺.

(R)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₂F₄N₄O₂)

To a solution of 4-fluoro-pyrazole (0.10 g, 0.001162 mol) in anhydrousTHF (10 mL), which was cooled in an ice water bath under an argonatmosphere, was added sodium hydride (60% dispersion in oil, 0.16 g,0.0040665 mol). After addition, the resulting mixture was stirred forthree hours.(S)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.41 g, 0.001162 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water, extracted with ethyl acetate.The organic layer was washed with brine, dried with MgSO₄, filtered, andconcentrated under vacuum. The product was purified by a silica gelcolumn using hexanes and ethyl acetate (2:1 to 1:1) as eluent to afford0.27 g (64%) of the titled compound as yellowish solid.

¹H NMR (400 MHz, DMSO-d₆) δ 10.38 (s, 1H, NH), 8.47 (d, J=1.6-2.0 Hz,1H, ArH), 8.24 (dd, J=8.4 Hz, J=2.0 Hz, 1H, ArH), 8.10 (d, J=8.4 Hz, 1H,ArH), 7.74 (d, J=4.4 Hz, 1H, Pyrazole-H), 7.41 (d, J=4.4 Hz, 1H,Pyrazole-H), 6.31 (s, 1H, OH), 4.39 (d, J=14.0 Hz, 1H, CH), 4.21 (d,J=14.4 Hz, 1H, CH), 1.34 (s, 3H, CH₃).

Mass (ESI, Positive): 357.11 [M+Na]⁺.

(S)-3-(4-Bromo-3-fluoro-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₁BrF₄N₄O₂) (1058)

To a solution of4-bromo-3-fluoro-1H-pyrazole (0.30 g, 0.001819 mol) inanhydrous THF (10 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.26g, 0.006365 mol). After addition, the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.64 g, 0.001819 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using ethyl acetate and hexanes (2:1) as eluent toafford 0.34 g (34%) of the titled compound as a pinkish solid.

¹H NMR (400 MHz, DMSO-d₆) δ 10.38 (s, 1H, NH), 8.45 (d, J=2.0-1.6 Hz,1H, ArH), 8.23 (dd, J=8.2 Hz, J=2.0 Hz, 1H, ArH), 8.11 (d, J=8.2 Hz, 1H,ArH), 7.82 (d, J=2.0 Hz, 1H. Pyrazole-H), 6.35 (s, 1H, OH), 4.35 (d,J=14.0 Hz, 1H, CH), 4.04 (d, J=14.0 Hz, 1H, CH), 1.37 (s, 3H, CH₃).

HRMS [C₁₅H₁₂BrF₄N₄O₂ ⁺]: calcd 435.0080, found 435.0080[M+H]⁺. Purity:96.98% (HPLC).

(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(3-fluoro-4-(4-fluorophenyl)-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₂₁H₁₅F₅N₄O₂) (1059)

The mixture of(S)-3-(4-bromo-3-fluoro-1H-pyrazol-I-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.20 g, 0.45% mmol). 4-fluoro boronic acid (77 mg, 0.5515 mmol),Pd(II)(OAc)₂ (2-3 mg, 0.009192 mmol), PPh₃ (7-8 mg, 0.02758 mmol), andK₂CO₃ (0.13 g, 0.965 mmol) in the mixture of ACN (4-5 mL) and H₂O (2-3mL) was degassed and refilled with argon three times. The resultingreacting mixture was heated at reflux for 3 hours under argon. Theproduct was purified by a silica gel column using hexanes and ethylacetate (2:1 to 1:1) as eluent to afford 51 mg (25%) of the titledcompound as a off-white solid.

¹H NMR (400 MHz, CDCl₃) δ 9.12 (s, 1H, NH), 8.06 (d, J=1.6 Hz, 1H, ArH),7.85 (dd, 8.2 Hz, J=1.6 Hz, 1H, ArH), 7.77 (d, J=8.2 Hz, 1H, ArH), 7.51(d, J=3.0 Hz, 1H, Pyrazole-H), 7.43-7.40 (m, 2H, ArH), 7.08-7.04 (m, 2H,ArH), 4.57 (d, J=10.5 Hz, 1H, CH), 4.7 (d, J=10.5 Hz, 1H, CH), 1.26 (s,3H, CH₃).

HRMS [C₂₁H₁₆F₅N₄O₂ ⁺]: calcd 451.1193. found 451.1196[M+H]⁺. Purity: %(HPLC).

(S)-3-(3-Bromo-4-cyano-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₆H₁₁BrF₃N₅O₂) (1060)

To a solution of3-bromo-4-cyano-1H-pyrazole (0.20 g, 0.0011629 mol) inanhydrous THF (10 mL) , which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.163g, 0.00407 mol). After addition. the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.41 g, 0.0011629 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using ethyl acetate and hexanes (2:1) as eluent toafford 0.10 g (20%) of the titled compound as an off-white solid.

¹ H NMR (400 MHz, DMSO-d₆) δ 10.32 (s, 1H, NH), 8.40 (s 1H, Pyrazole-H),8.41 (s, 1H, ArH), 8.20 (d, J=8.4 Hz, 1H, ArH), 8.11 (d, J=8.4 Hz, 1H,ArH), 6.47 (s, 1H, OH), 4.52 (d, J=13.6 Hz, 1H, CH), 4.33 (d, J=13.6 Hz,1H, CH), 1.41 (s, 3H, CH₃).

HRMS [C₁₆H₁₂BrF₃N₅O₂₊]: calcd 442.0126, found 442.0109[M+H]⁺. Purity:98.84% (HPLC).

(S)-3-(3-Chloro-4-methyl-1H-pyrazol-1-yl)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₆H₁₄ClF₃N₄O₂) (1061)

To a solution of 3-chloro-4-methyl-1H-pyrazole (0.15 g, 0.001287 mol) inanhydrous THF (10 mL) , which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.18g, 0.0045045 mol). After addition, the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.45 g, 0.001287 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using DCM and ethyl acetate (98:2 to 95:5) as eluentto afford 0.27 g (54%) of the titled compound as a white solid.

¹ H NMR (400 MHz, DMSO-d₆) δ 10.33 (s, 1H, NH), 8.42 (d, J=0.8 Hz, 1H,ArH), 8.21 (dd, J=8.4 Hz, J=0.8 Hz, 1H, ArH), 8.10 (d, J=8.2 Hz, 1H,ArH), 7.50 (s 1H, Pyrazole-H), 6.29 (s, 1H, OH), 4.36 (d, J=14.4 Hz, 1H,CH), 4.18 (d, J=14.4 Hz, 1H, CH), 1.91 (s, 3H, CH₃), 1.35 (s, 3H, CH₃).

HRMS [C₁₆H₁₅ClF₃N₄O₂ ⁺]: calcd 387.0836, found 387.0839[M+H]⁺. Purity:97.07% (HPLC).

(S)-3-(4-Fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methyl-N-(4-nitro-3-(trifluoromethyl)phenyl)propanamide (1062)

To a dry, nitrogen-purged 100 mL round-bottom flask equipped with adropping funnel under argon atmosphere. NaH of 60% dispersion in mineraloil (674 mg, 16.9 mmol) was added in 60 mL of anhydrous THF solvent inthe flask at ice-water bath, and 4-fluoro-1H-pyrazole (691 mg, 8.03mmol) was stirred in over 30 min at the ice-water bath. Into the flask,the solution of(R)-3-bromo-2-hydroxy-2-methyl-N-(4-nitro-3-(trifluoromethyl)phenyl)propanamide(2.98 g, 8.03 mmol) in 10 mL of anhydrous THF was added through droppingfunnel under argon atmosphere at the ice-water bath and stirredovernight at room temperature. After adding 1 mL of H₂O, the reactionmixture was condensed under reduced pressure, and then dispersed into 50mL of EtOAc, washed with 50 mL (×2) water, evaporated, dried overanhydrous MgSO₄, and evaporated to dryness. The mixture was purifiedwith flash column chromatography as an eluent EtOAc/hexane=1/2 toproduce designed compound (2.01 g, 67%) as yellowish solid.

MS (ESI) m/z 375.08[M−H]; 377.22 [M+H]⁺; 399.04 [M+Na]⁺;

¹⁹F NMR (CDCl₃, decoupled) δ −60.13, −176.47; assigned by NOE and COSY;¹H NMR (400 MHz, CDCl₃) δ 9.14 (bs, 1H, NH), 8.01 (s, 1H), 7.97-7.91 (m,2H), 7.38 (d, J=3.6 Hz, 1H), 7.35 (d, J=4.4 Hz, 1H), 5.95 (s, 1H, OH),4.56 (d, J=14.0 Hz, 1H), 4.17 (d, J=14.0 Hz, 1H), 1.48 (s, 3H).

(S)-3-(4-Fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanoic acid(1062a)

To a solution of 1062 (1.886 g, 5.29 mmol) in EtOH (40 ml) and water (20ml) was added NaOH (424 mg, 10.59 mmol) and the reaction mixture washeated to reflux for 2 h. evaporated (to remove the EtOH) and thenextracted with EtOAc. The aqueous phase was acidified to pH 1 andextracted with EtOAc. The extract was dried over Na₂SO₄, filtered andevaporated to afford the title compound (845 mg, 85%) as a brown oil. MS(ESI) m/z 187.06[M−H]; 188.91 [M+H]⁺;

¹⁹F NMR (acetone-d₆, decoupled) δ −0.24; assigned by NOE and COSY.

¹ H NMR (400 MHz, acetone-d₆) δ 7.66 (d, J=4.4 Hz, 1H), 7.36 (d, J=4.0Hz, 1H), 4.45 (d, J=14.0 Hz, 1H), 4.27 (d, J=14.0 Hz, 1H), 1.38 (s, 3H).¹³C NMR (100 MHz, acetone-d₆) δ 175.70, 150.36 (d, J=24.12 Hz),126.53(d, J=13.6 Hz), 118.21(d, J=28.0 Hz), 74.86, 60.59, 23.77.

Preparation of(S)-N-(6-Cyano-5-(trifluoromethyl)pyridin-3-yl)-3-(4-(4-fluorophenyl)-1H-1,2,3-triazol-1-yl)-2-hydroxy-2-methylpropanamide(1063)(S)-3-Azido-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(1064)

A solution of(R)-3-bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(352 mg, 1 mmol) in 10 mL of DMF was treated with NaN₃ (325 mg, 5 mmol)under Ar at 80° C. for 24 h. The reaction mixture was then cooled andextracted with CH₂Cl₂ (3×20 mL). The combined organic layers were washedwith H₂O (3×20 mL) and brine, dried and evaporated to give a crude oil,which purified by silica gel chromatography (EtOAc/n-hexane=1:2, v/v) toafford product. Yield=87%;

MS (ESI) m/z 313.03 [M−H]; ¹⁹F NMR (CDCl₃, decoupled) δ −62.11;

¹H NMR (400 MHz, CDCl₃) δ 9.16 (bs, 1H, NH), 8.89 (s, 1H), 8.77 (s, 1H),3.90 (d, J=12.0 Hz, 1H), 3.52 (d, J=12.0 Hz, 1H), 3.20 (bs, 1H, OH),1.55 (s, 3H).

(S)-N-(6-Cyano-5-(trifluoromethyl)pyridin-3-yl)-3-(4-(4-fluorophenyl)-1H-1,2,3-triazol-1-yl)-2-hydroxy-2-methylpropanamide(1063)

To a suspension of copper(I)iodide (11 mg, 0.055 mmoL) in acetonitrile(7 mL)/water (3 mL) mixture was added 1064 (57 mg, 0.182 mmol) at roomtemperature and then 1-ethynyl-4-fluorobenzene (0.015 mL, 0.182 mmol)was added. The resulting reaction mixture was stirred at roomtemperature for 3 days. The mixture was evaporated under reducedpressure, poured into water:brine (1:1) and then extracted with ethylacetate. The combined organic extracts were then washed with brine,dried over sodium sulphate, filtered and evaporated. Purification bychromatography (silica, 60% ethyl acetate in hexane) to afford theproduct as a yellow solid (51.3 mg, 65%).

MS (ESI) m/z 433.09[M−H] 435.06 [M+H]⁺;

¹⁹F NMR (acetone-d₆, decoupled) δ 114.58, 61.66; assigned by NOE andCOSY; ¹H NMR (400 MHz, acetone-d₆) δ 10.16 (bs, 1H, NH), 9.28 (s, 1H),8.88 (s, 1H), 8.31 (s, 1H), 7.90 (t, J=7.8 Hz, 2H), 7.20 (t, J=8.8 Hz,2H), 5.73 (bs, 1H, OH), 4.94 (d, J=14.2 Hz, 1H), 4.73 (d, J=14.2 Hz,1H), 1.62 (s, 3H).

(S)-3-(4-Bromo-3-fluoro-1H-pyrazol-1-yl)-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(1069)

To a solution of 4-bromo-3-fluoro-pyrazole (0.20 g, 0.0012124 mol) inanhydrous THF (10 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.17g, 0.0042434 mol). After addition, the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(0.327 g, 0.0012124 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄.filtered, and concentrated under vacuum. The product was purified by asilica gel column using hexanes and ethyl acetate (2:1 to 1:1) as eluentto afford 0.28 g (54%) of the titled compound as white solid.

HRMS [C₁₅H₁₂BrClF₃N₄O₂ ⁺]: calcd 434.9954, found 435.9997 [M+H]⁺.Purity: 93.41% (HPLC).

¹H NMR (400 MHz, DMSO-d₆) δ 10.67 (s, 1H, NH), 9.32 (d, J=2.0 Hz, 1H,ArH), 8.82 (d, J=2.0 Hz, 1H, ArH), 7.85 (d, J=2.0 Hz, 1H, Pyrazole-H),6.47 (s, 1H, OH), 4.35 (d, J=14.0 Hz, 1H, CH), 4.17 (d, J=14.0 Hz, 1H,CH), 1.39 (s, 3H, CH₃).

(S)-3-(3-Bromo-4-cyano-1H-pyrazol-1-yl)-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(1070) and(S)—N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-3-(4-cyano-3-phenyl-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide (1071)

(R)-3-Bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamideThionyl chloride (0.8 mL, 1.07 mol) was added dropwise to a cooledsolution (less than 4° C.) of (R)-3-bromo-2-hydroxy-2-methylpropanoicacid (1.27 g, 6.94 mmol) in 50 mL of THF under an argon atmosphere. Theresulting mixture was stirred for 3 h under the same condition. To thiswas added Et₂N (1.8 mL, 1.28 mmol) and stirred for 20 min under the samecondition. After 20 min, 5-amino-3-(trifluoromethyl)picolinonitrile (1g, 5.34 mmol) and 50 mL of THF were added, and then the mixture wasallowed to stir overnight at room temperature. The solvent was removedunder reduced pressure to give a solid which was treated with 50 mL ofH₂O and extracted with EtOAc (2×400 mL). The combined organic extractswere washed with saturated NaHCO₃ solution (2×50 mL) and brine (50 mL).The organic layer was dried over MgSO₄ and concentrated under reducedpressure to give a solid which was purified from column chromatographyusing CH₂Cl₂/EtOAc (80:20) to give a solid. This solid wasrecrystallized from CH₂Cl₂/hexane to give 1.32 g (70.2%) of(R)-3-bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamideas a light-yellow solid.

MS (ESI) m/z 351.08 [M−H]

¹⁹F NMR (CDCl₃, 400 MHz) δ −62.09.

¹H NMR (CDCl₃, 400 MHz) δ 9.15 (bs, 1H, NH), 8.90 (s, 1H), 8.78 (s, 1H),4.02 (d, J=10.8 Hz, 1H), 3.60 (d, J=10.8 Hz, 1H), 3.17 (bs, 1H, OH),1.66 (s, 3H).

(S)-3-(3-Bromo-4-cyano-1H-pyrazol-1-yl)-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2- methylpropanamide (1070)

To a dry. nitrogen-purged 50 mL round-bottom flask equipped with adropping funnel under argon atmosphere. NaH of 60% dispersion in mineraloil (232 mg, 5.81 mmol) was added in 10 mL of anhydrous THF solvent inthe flask at ice-water bath, and 3-bromo-1H-pyrazole-4-carbonitrile (500mg, 2.91 mmol) was added and stirred 30 min at the ice-water bath. Intothe flask,(R)-3-bromo-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(1.023 g, 2.91 mmol) in 10 mL of anhydrous THF was added throughdropping funnel under argon atmosphere at the ice-water bath and stirredovernight at room temperature. After adding 1 mL of H₂O, the reactionmixture was condensed under reduced pressure, and then dispersed into 50mL of EtOAc. washed with 50 mL (×2) water. evaporated, dried overanhydrous MgSO₄, and evaporated to dryness. The mixture was purifiedwith flash column chromatography as an eluent EtOAc/hexane =1/1, v/v toproduce the designed compound (1070, 1,043 g, yield 81%) as white solid.

MP 172.5-173.6° C.;

MS (ESI) m/z 442.1 [M−H]⁻; HRMS (ESI) m/z calcd for C₁₅H₁₀BrF₃N₆O₂443.0079 [M+H]⁺ found 443.0083 [M+H]⁺; 464.9903 [M+Na]⁺;

¹⁹F NMR (CDCl₃, 400 MHz) δ −61.25; The structure of product wasconfirmed with 2D NMR (COSY and NOESY);

¹H NMR (DMSO-d₆, 400 MHz) δ 10.60 (bs, 1H, NH), 9.29 (s, 1H), 8.79 (s,1H), 8.53 (s, 1H), 6.59 (s, OH), 4.50 (d, J=14.0 Hz, 1H), 4.32 (d,J=14.0 Hz, 1H), 1.43 (s, 3H).

(S)-N-(6-Cyano-5-(trifluoromethyl)pyridin-3-yl)-3-(4-cyano-3-phenyl-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(1071)

A flask equipped with a reflux condenser, a septum inlet and a magneticstirring bar was charged with(S)-3-(3-bromo-4-cyano-1H-pyrazol-1-yl)-N-(6-cyano-5-(trifluoromethyl)pyridin-3-yl)-2-hydroxy-2-methylpropanamide(1070, 53 mg, 0.23 mmol), tetrakis(triphenylphosphine) palladium (0) (9mg, 0.07 mmol), and phenyl boronic acid (35 mg, 0.28 mmol) in THF/MeOH(5 mL/1 mL) with sodium carbonate (50 mg, 0.48 mmol) in deoxygenatedwater (1 mL), and was stirred and heated to reflux for 2 h untilbromopyrazole was not detectable on TLC. The mixture was cooled to roomtemperature and the solvent was removed in vacuo and then poured intoEtOAc (10 mL), and extracted with EtOAc. The combined organic layerswere washed with sat. NH₄Cl, water and dried over MgSO₄. The solvent wasremoved in vacuo and then purified by flash column chromatography onsilica gel using EtOAc/hexane (1/1, v/v) as an eluent to give thetargeted compound (1071. 36 mg, 69%) as yellowish solid.

MP 112.3-124.4° C.;

MS (ESI) m/z 439.2 [M−H]⁻; HRMS (ESI) m/z calcd for C₂₁H₁₅F₃N₆O₂441.1287 [M+H]⁺ found 441.1291 [M+H]⁺; 463.1111 [M+Na]⁺:

¹⁹F NMR (CDCl₃, 400 MHz) δ −62.09; The structure of product wasconfirmed with 2D NMR (COSY and NOESY):

¹H NMR (CDCl₃, 400 MHz) δ 9.17 (bs, 1H, NH), 8.76 (s, 1H), 8.60 (s, 1H),7.77 (s, 1H), 7.57-7.52 (m, 3H), 7.18 (d, J=8.8 Hz, 2H), 5.32 (s, OH),4.60 (d, J=14.0 Hz, 1H), 4.23 (d, J=14.0 Hz, 1H), 1.47 (s, 3H).

Example 14 SARDs Regressed CPRC VCaP Tumors

VCaP prostate cancer cells were implanted (in combination with matrigel(1:1 mix)) on the flanks subcutaneously in SRG rats (10 millioncells/rat). When the tumors reach 300-500 mm³. the animals werecastrated and the tumors were allowed to regrow as castration-resistantprostate cancer. When the tumors regrew, the animals were randomizedinto three groups, vehicle (15% DMSO+85% PEG-300), enzalutamide (30mg/kg/day), or compound 1002 (60 mg/kg/day). The animals were orallytreated and tumor volume and body weight were recorded thrice weekly.Tumor volume or percent change in tumor volume was calculated.

Vehicle-treated tumors grew robustly in castrated environment indicatingthat the tumors were castration-resistant, i.e., tumor were CRPC.Enzalutamide inhibited the growth of the tumors, while compound 1002regressed the tumors to undetectable levels (FIG. 35A). All individualanimals treated with 1002 had tumor volume reduced to unmeasurable by 22days (FIG. 35B), whereas enzalutamide response was more variable andincomplete even at 30 days.

Example 15 SARDs Inhibited Growth of Tumor and Caused Rapid TumorRegression in Anti-androgen Resistant (MDVR) VCaP cells in Intact andCastrated Animals

VCaP cells that have been rendered enzalutamide resistant were implanted(in combination with matrigel (1:1 mix)) on the flanks subcutaneously inSRG rats (10 million cells/rat). When the tumor reached 10,800 mm³, theanimal was treated orally with compound 1002 (60 mg/kg/day) to determineif the tumor growth is slowed. Tumor volume and body weight was recordedthrice weekly.

Animal No. 803 was cryptorchid and there were complications upon tryingto remove testes, so the animal was left intact. Before initiation of1002 treatments, the MDV3100 (enzalutamide) resistant (MDVR) VCaP cellsgrew robustly, presumably supported by the endogenous androgens. 1002quickly inhibited growth and caused rapid tumor regression, however, theanimal was sacrificed due to loose stools (FIG. 36). Interestingly, theresponse to treatment in this animal was rapid despite the androgenreplete milieu of an intact rat. E.g., FIG. 36A demonstrates that as thetumor began to grow, the serum PSA levels began to rise as shown by thenumbers above each time point in the tumor volume graph (left panel inFIG. 36A), however, immediately after initiation of 1002 treatments thePSA levels fell to zero.

In the right panel of FIG. 36A, serum PSA levels are graphed (numberprovided on the graph are serum PSA values (ng/mL); blood was obtainedweekely and serum separated and stored for PSA analysis; tumor volumewas measured thrice weekly) for this animal allowing visualization ofthe dramatic rise in PSA with tumor growth and rapid PSA response uponinitiation around day 58. By comparison in FIG. 36B, vehicle treated andenzalutamide treated animal experienced rapid tumor volume increases.This is preliminary evidence that SARDs of this invention can overcomeenzalutamide resistance in the presence of androgens and that the rapidtumor response is based on blocking the AR-axis. This provided theinspiration to test MDVR xenografts in intact animals. The experimentwas repeated with three rats per group and the same result was observed.Rapid and robust tumor response in MDVR VCaP tumors in intact ratstreated with 1002 and rapid progression in enzalutamide and vehicletreated intact rats (FIG. 37). This is the first evidence that an ARantagonist can inhibit CRPC tumor growth in an intact animal species(rat). This result provides evidence that SARDs of this invention can beused to treat prostate cancer even in the presence of endogenous agonist(i.e., intact animals) which is an unexpected result and differs fromthe standard of care in which the first pharmacotherapy is typicallyandrogen-deprivation therapy. Although this result is in an enzalutamideresistant CPRC, it provides a basis for testing in early prostatecancers and suggests the possibility of adjuvant or neoadjuvant use ofSARDs of this invention in intact men.

MDVR VCaP Xenograft Growth in Castrated Rats: MDVR VCaP prostate cancercells were implanted (in combination with matrigel (1:1 mix)) on theflanks subcutaneously in SRG rats (10 million cells/rat). When thetumors reach 300-500 mm³, the animals were castrated and the tumors wereallowed to regrow as castration-resistant prostate cancer. When thetumors regrew, the animals were randomized into three groups. vehicle(15% DMSO+85% PEG-300), enzalutamide (30 mg/kg/day), or compound 1002(60 mg/kg/day). The animals were orally treated and tumor volume andbody weight were recorded thrice weekly. Tumor volume or percent changein tumor volume was calculated.

Vehicle-treated tumors grew robustly in castrated environment indicatingthat the tumors were castration-resistant, i.e., tumor were CRPC.Enzalutamide treated tumors also continued to grow almost comparably tovehicle, while compound 1002 regressed the tumors to inhibited tumorgrowth significantly (FIG. 38) with tumor at sacrifice (approximatelyday 26) slightly smaller than at initiation of treatment or 2000 mm³. Bycomparison, vehicle and enzalutamide tumor grew by from 2000 mm³ to 6000mm³ or 200% increased tumor volume. This demonstrated that SARDs of thisinvention are able to treat antiandrogen resistant castration resistantprostate cancer (MDVR VCaP) which over expresses CYPI7A I such thatthere is intratumoral androgen synthesis as well. Correspondingly, SARDsof this invention are expected to he able to treat CRPC (and possiblyCSPC) including patients that have failed enzalutamide or apalutamideand possibly abiraterone treatments, or patients overexpressing CYP17A1or AKR1C3.

Example 16 X-Linked Spinal-Bulbar Muscular Atrophy (SBMA) Method

Transgenic mice that express AR121Q (121 polyglutamine repeats insteadof the usual 15-24 repeats) will be treated with vehicle or SARD orally.One group of mice will be castrated to serve as positive control ascirculating androgens will worsen the SBMA condition. Body weight,composition, and grip strength will be measured before the initiation ofthe experiment. Animals will be treated and weekly measurements will beperformed. Animals will be treated and monitored until they die. AR121Qmice lives only up to 60-80 days and hence evaluating the survival inthe presence of SARD treatment is possible.

Example 17 ALS Method

All experiments will be performed in male hSOD1-G93A mice (Jax labs;PMID: 26786249) as a model of anterior lateral sclerosis (ALS). Micewill be randomized and treated with either vehicle or SARD of thisinvention dissolved in DMSO+PEG-300 (15%+85%). Simultaneously, a groupof mice will be castrated and used as positive control as castration hasbeen shown to extend survival and disease duration in this model (PMID:24630363). Mice will be treated orally every day until they reachmorbidity. Weekly body weight and composition by magnetic resonanceimaging (MRI) will be recorded. The mice performance will be measuredeach week by using a grip strength meter (Columbus instruments) orrotarod. Inability for the mice to move will be considered as a terminaldisease state and the mice will be sacrificed.

Example 18 1002 as an Orally-Bioavailable Selective Androgen ReceptorDegrader: Potential Next-Generation Therapeutic forEnzalutamide-Resistant Prostate Cancer

(Some of the experiments of Example 18 can also be found, in part, inother examples herein such as Examples 1, 3-7, 9-12, 14 and 15, but arepresented in a more complete and cohesive fashion in Example 18.Literature references in this section are called out by sequentialnumbers and listed at the end of Example 18.)

Abstract: Androgen receptor (AR)-targeting prostate cancer drugs, whichare competitive ligand binding domain (LBD)-binding antagonists, areinactivated by common resistance-mechanisms. It is important to developnext-generation mechanistically-distinct drugs to treat castration- anddrug-resistant prostate cancers. Here, we have discovered asecond-generation AR to pan-antagonist (1002) that binds to theactivation function-1 domain (AF-1) of the AR and degrades the AR and ARsplice variants. 1002 inhibits the wildtype and LBD mutant ARscomparably and inhibits the proliferation and growth ofenzalutamide-sensitive and resistant prostate cancer xenografts. Inpreclinical models. 1002 regresses enzalutamide-resistant tumors tounmeasurable levels at doses when the AR is degraded but completelyinhibits, but not regresses, the tumors at lower doses when the AR isantagonized, and not degraded. This is the first indication thatdegradation might provide a complete tumor regression. Mechanistically,1002 promotes a conformation of AR that is distinct from the LBD-bindingcompetitive antagonist, enzalutamide, and degrades the AR through theubiquitin proteasome mechanism. Early toxicology studies suggest that1002 is safe and has a broad safety margin. Collectively, 1002 exhibitsthe properties necessary for a next-generation drug for the treatment ofadvanced prostate cancer.

Introduction: About 3.3 million men are surviving with prostate cancer(PCa) in the United States and this number is expected to increase to4.5 million by 2026 [1]. In addition to radical prostatectomy combinedwith gonadotrophins, androgen-synthesizing enzyme inhibitor and androgenreceptor (AR) antagonists have been the mainstay of PCa treatmentparadigm [2, 3]. PCa that progresses after initial treatment choices,called castration-resistant prostate cancer (CRPC), grows rapidly andmetastasizes to distant organs [4, 5]. Three targeted treatments,enzalutamide and apalutamide. AR antagonists, and abiraterone, anandrogen-synthesizing enzyme inhibitor, which have been approved in thelast 5-10 years to combat CRPC, provided clear evidence that the CRPC,despite being castration-resistant, is still dependent on the AR axisfor continued growth [2, 3].

About 30-40% of CRPCs fail to respond to enzalutamide or abiraterone [2,3, 6, 7], while the remaining develop resistance after a brief period ofresponse [8]. Although several potential mechanisms for the resistancedevelopment have been identified, mutations in the AR ligand bindingdomain (LBD) and expression of AR splice variants (AR-SVs) have beenbroadly shown in the clinic [9, 10]. AR antagonists in the market(enzalutamide and apalutamide) and in clinical trials (darolutamide) areall competitive antagonists and do not mechanistically differ from eachother. Abiraterone manipulates the levels of endogenous LBD targetedandrogens and is cross-resistant with the enzalutamide conferring pointmutations discussed below. Hence, all AR targeted therapy relies on LBDfor suppression of the AR-axis.

AR is a member of the steroid receptor family of ligand-activatedtranscription factors. Structurally, AR, like other steroid receptors,contains an N-terminus domain (NTD) that expresses an activationfunction-1 (AF-1) domain, a DNA-binding domain (DBD) that recognizeshormone response elements (HREs), a hinge region, and a ligand-bindingdomain (LBD) that contains an AF-2 [11]. The AF-1 contains twotranscription activation regions, tau-1 and tau-5, which retain themajority of the AR function. Drugs that target the steroid receptors actby predominantly binding to the LBD. Prolonged treatment with ARantagonists results in mutations in the LBD, leading to resistance. W741mutation to leucine or cysteine in the AR leads to resistance tobicalutamide [12], while F876 mutation to leucine confers resistance toenzalutamide and apalutamide [9, 13, 14].

While mutations in the AR LBD can be ideally overcome with antagoniststhat bind to the LBD in a distinct conformation, resistance due toAR-SVs confers a serious challenge due to the absence of the LBD.Current AR-targeting drugs that bind to the LBD will be unable toinhibit AR-SV function. AR-SVs have been shown to be responsible foraggressive CRPC phenotype, shorter overall survival, and failure of thecancer to respond to AR-targeted treatments or to chemotherapeuticagents [10, 15-18]. Although most of the recent studies on PCaresistance have focused on AR-SVs, activation of other pathways are alsoconsidered to play roles in resistance development [19, 20].

Although degraders of estrogen receptor have been successfullydiscovered [21, 22], for unknown reasons, AR degraders have not beendeveloped yet. Degraders confer added advantage of preventing ARactivation by alternate signaling pathways and by intra-tumoralandrogens and hence might provide a sustained treatment option for CRPC.As AR and AR-SVs are detected as heterodimer in the clinic, it isbelieved that degrading the AR could potentially result in AR-SVdegradation [23]. Discovery of PROTACs and small molecules from ourgroup has provided some confidence that AR degraders could he developedusing alternate strategies [24-27]. Unfortunately, the PROTACs are largemolecules with molecular weights greater than 1000 Da and hence mightnot possess ideal drug-like properties and our first generationmolecules have poor oral bioavailability and hence lack drug-likeproperties. It is also important to develop molecules that hind todomains other than the LBD [26, 28] to inhibit AR-SVs and to overcomeresistance due to mutations in the LBD.

Here we report the discovery of a novel small molecule pan-antagonistand degrader. 1002, a second-generation molecule, that hinds to the AR,and degrades wildtype, enzalutamide-resistant, and splice-variant ARs.1002, which possesses appropriate pharmacokinetic (PK) properties, waseffective in various in vivo models. 1002 inhibited androgen-dependenttissues such as prostate and seminal vesicles in rats and growth ofenzalutamide-resistant CRPC xenografts. 1002 also potently regressedtumors in intact immunocompromised rats, data that has not been observedbefore with competitive antagonists due to their inability to competewith the abundant circulating testosterone. These data provide the firstevidence of the potential of an orally-bioavailable AR degrader inadvanced prostate cancer.

Materials and Methods.

Reagents. The source of the several reagents used in this example hasbeen described previously [26, 27]. ³H mibolerone and R1881 werepurchased from Perkin Elmer (Waltham, Pa.). Enzalutamide was obtainedfrom MedKoo (Morrisville, N.C.). Dual- luciferase and CellTiter-Gloassay reagents were procured from Promega (Madison, Wis.). AR (N20 andC19), mono- and poly-ubiquitin (SC-8017), and glucocorticoid receptor(GR) antibodies were obtained from SantaCruz Biotechnology (SantaCruz,Calif.). AR PG-21 antibody was obtained from Millipore (Burlington,Mass.). Dihydrotestosterone (DHT), dexamethasone, GAPDH antibody, andcycloheximide were procured from Sigma (St. Louis, Mo.). Progesteronereceptor (PR) and estrogen receptor (ER) antibodies were obtained fromCell Signaling (Danvers, Mass.). Bortezomib was procured fromSelleckchem (Houston, Tex.). AR-V7 antibody and serum PSA kit wereprocured from Abcam (Cambridge, UK). Lipofectamine and TaqMan primersand probes and real time PCR reagents were purchased from LifeTechnologies (Carlsbad, Calif). HA (hemagglutinin) antibody waspurchased from Novus Biologicals (Littleton, Colo.). 17-AAG (MedChemExpress) and doxycycline were procured from Fisher Scientific (Hampton,N.H.). Liver microsomes were obtained from Xenotech LLC (Kansas city,Kans.). DAPI was obtained from Vector Laboratories (Burlingame, Calif.).MG-132 was purchased from R&D Systems (Minneapolis, Minn.).

Cell Culture. LNCaP, PC-3, HEK-293, 22RV1, and COST cell lines wereprocured from the American Type Culture Collection (ATCC, Manassas,Va.). All cells were cultured in accordance to ATCC recommendations.LNCaP cell line stably transfected with doxycycline-inducible AR-V7 wasa kind gift from Dr. Nancy L. Weigel (Baylor College of Medicine,Houston, Tex.) [29, 30]. Enzalutamide-resistant MR49F cells were a kindgift from Dr. Martin Gleave (University of British Columbia, Vancouver).Enzalutamide-resistant VCaP cells (MDVR) were licensed from Dr. DonaldMcDonnell (Duke University, N.C.). All cell lines were authenticated byshort terminal DNA repeat assay (Genetica Cell Line Authenticationtesting, Burlington, N.C.).

Chromatin Immunoprecipitation Assay (ChIP). ChIP assays were performedas described previously [26, 31-33] and under the conditions describedin the figures. Briefly, proteins were cross-linked to DNA using 1%formaldehyde and incubated at room temperature for 10 min. Medium wasaspirated from cell culture dishes and washed twice with ice cold PBS.Cells were lysed in a lysis buffer containing protease and phosphataseinhibitors. DNA was fragmented by sonication using a probe sonicator andthe respective proteins were immunoprecipitated with selectiveantibodies. The protein-antibody complex was pulled down using magneticbeads (Dynabeads, Life Technologies), the complex was reversecross-linked at 65° C. for 6 hours, and the DNA was purified. Primersand fluorescent probes for realtime PCR were described previously [26,29, 30].

Gene expression. RNA extraction and cDNA preparations were performedusing cells-to-ct kit. Gene expression studies were performed usingTaqMan probes on ABI 7900 realtime PCR machine.

Growth Assay. Growth assay was performed using CellTiter-Glo orsulforhodamine blue (SRB) reagents.

Plasmid constructs and transient transfection. Many plasmids (CMV hAR,AR-LSD, PR, GR, MR, ER, GRE-LUC, CMV-LUC, AR AF-1, and AR NTD plasmids)used in the study were described earlier [26, 32, 33]. Mouse AR, rat GR,GAA (GR-NTD, AR-DBD and AR-LBD), and AGG (AR-NTD, GR-DBD and GR-LBD)were kind gifts from Dr. Diane Robins 1341. Constructs dtau1 (tau-1deleted AR), dtau5 (tau-5 deleted AR), and AR-NTD-DBD were kind giftsfrom Dr. Frank Claessens [35, 36]. Transfections were performed usingLipofectamine reagent (Life Technologies. Carlsbad, Calif.).

Competitive ligand binding assay: Ligand binding assay with purifiedGST-tagged AR-LSD and ³H mibolerone was performed as describedpreviously [26]. Whole cell ligand binding assay was performed using themethod described previously [37]. Briefly, COS cells were plated in 24well plates at 100,000 cells/well in DME +5% csFBS without phenol redmedium. Cells were transfected with the indicated amounts of hAR-LBDusing lipofectamine reagent. Cells were treated with a dose response ofthe compounds in the presence of ³1H mibolerone. Cells were washed fourhours after treatment with ice cold PBS and the intracellular proteinsand radioactive mibolerone were extracted using ice cold 100% ethanol.Radioactivity was counted using a scintillation counter.

Western blotting and immunoprecipitation. Cells were plated in 60 mmdishes in growth medium. Medium was changed to the respective mediumdescribed in the figures and treated with compounds under variousconditions. Protein extracts were prepared and Western blot wasperformed as described earlier [32, 33]. Immunoprecipitation wasperformed using protein AIG agarose.

Fluorescence polarization (FP). FP studies were performed with GST-AF-1and GST-NTD purified protein as described earlier 1281.

1002 NTD binding assay. ³H-1002 was synthesized at Perkin Elmer fromiodinated 1002 precursor. HEK-293 cells were transfected with 1 μg ofthe indicated plasmids using lipofectamine. Twenty-four hours aftertransfection, the cells were fed with growth medium. The cells wereharvested 48 hours after transfection and protein was extracted. Theprotein extract was incubated with 5 μM ³H-1002 in an AR-binding assaybuffer at 4° C. for 16 hours. The reaction mixture was added to G25Sephadex column (GE Life Sciences, PD-10 columns Cat. No. 17085101) toseparate the unbound radioactive nucleotides from labeled compound boundto the protein. The amount of radioactive material incorporated in theprotein was counted using a scintillation counter.

Demonstration of NTD binding proved difficult as chronicled below due tothe lack of any precedent regarding how the assay should he formulatedand the absence of any high affinity NTD binding ligands to use asstandard agents. Finally, the addition of G25 Sephadex column reducedthe background (unbound) radiation to allow observation of NTD boundradiation (³H-1002 NTD binding) and its displacements by cold NTD ligand(1002).

Standard NTD ligands need to bind to NTD only (i.e., not LBD also) andbind to NTD reversibly such that it could be displaced. In the absenceof any prior art NTD ligand of the above description, ³H-1002 wassynthesized and used for this purpose even though its properties werenot optimal (e.g., NTD binding affinity was not known but not believe tobe low nM affinity like LBD standard agents) to serve as a standardagent. Correspondingly, formulating the competitive NTD binding assaystill proved difficult. Multiple iterations were required in order tofigure out how to produce an assay that reduces the background radiationenough to see NTD binding which multiple biochemical and biophysicalmethods reported herein all suggest.

Failed attempts to demonstrate NTD binding using displacement of ³H-1002

Experiment 609. Aug. 24, 2017

COS cells were plated in 24 well plates at 90,000 cells per well in DMEM+5% charcoal stripped-fetal bovine serum (csFBS) without phenol red.After overnight, changed medium to OptiMEM (0.25 ml). The cells weretransfected with vector, AR-LBD, AR-NTD, or full length AR. The cellswere treated with ³H-1002 for 48 h after transfection and were harvested4 h after treatment. After incubation, the cells were washed 3 timeswith ice cold PBS to remove unbound hormone. Bound hormone was extractedusing 100% ice-cold ethanol, and counted on Beckman scintillationcounter (Alaina James, Weigel, Mol Endo paper on A748T mutation).10{circumflex over ( )}-5 M=3.1 μL/0.5 mL medium.

Reason for failure. High background precluded the detection of anybinding.

Experiment 625. Sep. 21, 2017

HEK-293 cells were plated in 60 mm dishes at 2 million cells per dish inDMEM +5% csFBS without phenol red. After overnight, medium was changedto OptiMEM (1 mL). The dishes were transfected vector or AR full length.The cells were treated with 10 μM ³H-1002 for 24 hrs after transfectionand were harvested 4 h after treatment, and immunoprecipitated with theAR antibody (AR PG 21) was performed. Gel was run and the gel piecebetween 70 and 120 kDa was cut and counted in a scintillation counter.

Reason for failure. High background precluded the detection of anybinding.

Experiment 640. Oct. 2, 2017

HEK-293 cells were plated in 60 mm dishes at 2 million cells per dish inDMEM +5% csFBS without phenol red. After overnight, medium was changedto OptiMEM (1 mL). The dishes were transfected with either vector orfull length AR. The cells were treated with ³H-1002 24 h aftertransfection and were fixed with 4% formaldehyde for 2 h aftertreatment, harvested, and immunoprecipitated with AR antibody (AR PG 21)was performed. The immunoprecipitated beads were counted in ascintillation counter.

Reason for failure. High background precluded the detection of anybinding.

Experiment 647. Oct. 7, 2017

HEK-293 cells were plated in 60 mm dishes at 2 million cells per dish inDMEM +5% csFBS without phenol red. After overnight, medium was changedto OptiMEM (1 mL). The dishes were transfected with either vector orfull length AR. The cells were treated with ¹H-1002 alone or incombination with 100 fold excess of cold 1002 or R1881 (in order toreduce the counts to prove that there is binding) 24 h aftertransfection and were fixed with 4% formaldehyde for 2 h aftertreatment, harvested, and immunoprecipitated with AR antibody (AR PG 21)was performed. The immunoprecipitated beads were counted in ascintillation counter.

Reason for failure. No binding detected

Experiment 652. Oct. 12, 2017

HEK-293 cells were plated in 150 mm dishes at 5 million cells per dishin DMEM +5% csFBS without phenol red. After overnight, medium waschanged to OptiMEM (10 mL). All the dishes were transfected with AR fulllength. Twenty four hours after transfection, medium was changed to DME+5% csFBS without phenol red and were allowed to incubate for 24 hours.Cells were harvested 48 h after transfection, protein extracted, and theprotein extracts were used for in vitro binding assay with ³H-1002.

Binding assay.

-   -   (a) Incubated the protein extract with ³H -1 00 2 alone or in        combination with cold compounds at 4° C. on ice for 16 h.    -   (b) 200μL hydroxyapatite was added, vortexed, and incubated on        ice for 30 min. Centrifuged at 2000 g for 5 min.    -   (c) Washed 3× with Tris buffer (50 mM pH 7.4). Vortexed after        each wash and centrifuged at 2000 g for 5 min.    -   (d) Eluted with 1 mL of 100% cold ethanol. Incubated at room        temperature for 30 min.    -   (e) Centrifuged and added the supernatant to scintillation vials        with 10 mL scintillation cocktail and counted. Results. No        binding was detected

Experiment 684. Nov. 26, 2017

COS cells were plated in 24 well plates at 90,000 cells per well in DMEM+5% csFBS without phenol red. After overnight, change medium to OptiMEM(0.25 mL). The cells were transfected with vector, AR full length, orAR-LBD. The cells were treated with ³H-1002 or ³H-mibolerone for 24 hafter transfection and were harvested 4 h after treatment. The cellswere washed 3 times with ice cold PBS to remove unbound hormone. Boundhormone was extracted using 100% ice-cold ethanol, and counted onBeckman scintillation counter (Alaina James, Weigel . Mot Endo paper onA748T mutation). 10{circumflex over ( )}-5 M=3.1 ul/0.5 ml medium.

Results. While ³1-1-mibolerone showed binding to both AR-LBD and AR fulllength, ³H-1002 failed to bind to either construct.

In view of the absence of standard ligand and the absence of knownmethodology, the composition of matter ¹H-1002 and its use for detectingNTD binding are regarding as non-obvious and outside the skill of theordinarily skilled artisan.

Thermal-shift assay. Thermal-shift assay was performed using InCellpulse kit from DiscoverX (Fremont, Calif.; Cat. No. 94-4007). AR-NTD andAR-LBD were cloned in-frame into pICP-cPL-N and pICP-ePL-C vectors. Theplasmid constructs were evaluated for their activity. The N vectorplasmids provided the optimum activity and hence were selected for theassays. Forty pL of transfected cells (5000 cells) in assay medium wereadded to each well of a 96 well plate. Cells were treated with compoundor vehicle, and incubated for 1 h at 37° C. with 5% CO₂ incubator. Thencells were incubated for 3 minutes with gradient temperature from 39 to59° C. in a thermocycler to identify thermal denaturation temperaturesfor the sensitive detection of cellular target engagement. Forty μL ofassay reagent, which contains the enzyme acceptor, lysis buffer andsubstrate were added to each well and incubated for 60 minutes at roomtemperature. The samples were read on a luminometer at 1.0 seconds perwell.

Microarray. MR49F cells were maintained in 1% charcoal-strippedserum-containing medium for 2 days. Medium was changed again and thecells were treated with vehicle, 0.1 nM R1881 alone, or in combinationwith 10 μM 1002 (n=3-4/group). Twenty four hours after treatment, thecells were harvested. RNA was extracted, and was subjected to microarrayanalysis (University of Tennessee Health Science Center (UTHSC)Molecular Resources Center). Clarion S array was processed as describedpreviously 1261 and the data was analyzed using One Way ANOVA. Genesthat were 1.5 fold different from the comparator group and a falsediscovery rate (FDR) with q<0.05 were considered for further analysis.Ingenuity Pathway Analysis (IPA) was performed to determine thecanonical pathway and the diseases represented by the enriched genes.

Mice Xenograft experiment. All animal studies were conducted under UTHSCanimal care and use committee (ACUC) approved protocols. NOD SCID Gamma(NSG) mice were housed as five animals per cage and were allowed freeaccess to water and commercial rodent chow. Cell line xenografts wereperformed as previously published [33, 38]. LNCaP enzalutamide-resistant(MR49F) cells were implanted subcutaneously in intact mice(n=8-10/group). Once the tumors reach 100-200 mm³, the animals werecastrated and the tumors were allowed to regrow as castration-resistanttumors. Once the tumors reach 200-300 mm³ post castration, the animalswere randomized and treated orally with vehicle (polyethyleneglycol-300: DMSO 9:1 ratio) or 1002. Tumors were measured twice tothrice weekly and the volume was calculated using the formulalength*width*width*0.5236. Animals were sacrificed at the end of thestudy and the tumors were weighed and stored for further processing.

Rat xenograft experiments. Rat xenograft experiments were performed inSRG (Sprague Dawley-Rag2:IL2rg KO) rats at Hera Biolabs (Lexington,Ky.). Rats were inoculated subcutaneously with 10 million cells in 50%matrigel. Once the tumors reached 1000-2000 mm³. the animals were eitherrandomized and treated (intact) or were castrated and the tumors wereallowed to grow as CRPC. Once the tumors attain 2000-3000 mm³, theanimals were orally treated as indicated in the figures. Tumor volumeswere recorded thrice weekly. Blood collection and body weightmeasurements were conducted weekly once. At sacrifice, tumors wereweighed and stored for further analyses.

Hershberger assay. Male mice or rats (6-8 weeks old) were randomizedinto groups based on body weight. Animals were treated orally asindicated in the figures for 4 or 13 days. Animals were sacrificed,prostate and seminal vesicles were weighed, and represented as organweights normalized to body weight.

Metabolic stability. Metabolic stability studies in microsomes fromvarious species were conducted as described previously [26].

Statistics. Statistical analysis was performed using Graphpad prismsoftware. T-test was used to analyze data from experiments containingtwo groups, while One Way analysis of variance (ANOVA) was used toanalyze data from experiments containing more than two groups.Appropriate post hoc test was used to analyze data that demonstratedsignificance in ANOVA. Statistical significance are represented as *p<0.05; ** p<0.01; *** p<0.001.

Results: Our first generation SARDs, 17 and 11, were excellent degraderswith unique mechanistic properties [26]. Unfortunately, theirpharmacokinetic (PK) properties were not appropriate for furtherdevelopment. Oral administration of 11 in rats for 14 days failed tosignificantly inhibit the seminal vesicles weight (FIG. 39A) at 100mg/kg, while in LNCaP xenograft tumor-bearing NSG mice failed to inhibitthe tumor growth (FIG. 39B). Mouse and human liver microsomes data alsoshow rapid clearance and short half-life (FIG. 39C). Hence, we continuedour pursuit to develop molecules, that retain the degradation andantagonistic characteristics of the first generation molecules but willhave better PK properties. 1002 (FIG. 40A) satisfies these requirementsand was selected from a library for further characterization. Moreover,we focused on enzalutamide-resistant CRPC models with a view to developit for enzalutamide-resistant CRPC and these tumors tend to bepan-resistant and untreatable.

1002 inhibits wildtype and mutant ARs comparably. 1002 was first testedin a binding assay using in vitro purified AR-LBD binding assay [26].1002 failed to hind to the purified AR-LBD and displace 1 nM ³Hmibolerone (FIG. 40B left panel). To verify the result obtained inpurified AR-LBD, we performed whole cell ligand binding assay in COScells transfected with AR-LBD and treated with a dose response of 1002in combination with 1 nM ³H mibolerone. 1002 displaced ³H mibolerone,although its binding was much weaker (inhibition observed only at 10 μM)than that of enzalutamide or 11 (FIG. 40B). The conflicting resultbetween purified AR-LBD and whole cell binding assays could he due tomany possibilities that include potential stabilization of the1002-AR-LBD complex by intracellular factors or faster on-off rate of1002 in the ligand binding pocket in the absence of stabilizationfactors precluding detection of binding, or requirement of additionalfactors to bind to the AR-LBD. These questions need to be resolved infuture studies.

We next determined the antagonistic property of 1002 in wildtype and LBDmutant ARs and compared the results to the effect of enzalutamide (FIG.40C and Table 5). COS cells were transfected with wildtype or mutantARs, GRE-LUC, and CMV-renilla LUC and a luciferase assay was performed.1002 antagonized the wildtype AR with IC₅₀ around 200 nM, whileenzalutamide antagonized around the same concentration. 1002 comparablyor with better IC₅₀ inhibited the various mutant ARs (W741L. T877A, andF876L). Enzalutamide was weaker in W741L by 4-5 fold, and behaved as anagonist in F876L AR as reported earlier [9, 14].

TABLE 5 Binding, pan-antagonism of AR and steroid receptor antagonisticselectivity of 1002. Transactivation (IC₅₀ nM) GR MR Ki (nM) AR T877AW741L PR μM μM 1002 N.B 203.46  80.78  94.17 1092 >10 >10 Enza >1000183.41- 54.91 619.73 196.97 >10 >10 374.62  Binding of 1002 to purifiedAR-LBD was determined by cell-free competitive radiolabeled bindingassay. Transactivation assays were performed using wildtype or mutantARs, and PR, GR, or MR. Cells were transfected with the indicatedreceptors, GRE-LUC, and CMV-renilla LUC. Cells were treated with a doseresponse between 1 pM and 10 μM and luciferase assay was performed 24 hafter treatment. N.B. No binding. AR-androgen receptor; PR-progesteronereceptor; GR-glucocorticoid receptor; MR-mineralocorticoid receptor;T877A-Threonine 877 of AR mutated to alanine; W741L-tryptophan 741 of ARmutated to leucine.

1002 degrades wildtype and F876L). Enzalutamide-resistant ARs. As theobjective was to develop degraders of the AR. Western blot was used as ascreening tool in our discovery paradigm. We tested the effects of 1002on AR protein level in LNCaP cells and in enzalutamide-resistant MR49Fcells. LNCaP or MR49F maintained in charcoal-stripped serum-containingmedium were treated with a dose response of 1002 in the presence of 0.1nM R1881 for 24 h. Cells were harvested, protein extracted, and Westernblot for AR was performed. Treatment of LNCaP cells with 1002 resultedin a reduction of the AR levels in LNCaP cells with down-regulationobserved at 1000 nM (FIG. 41A left panel). While 1002 resulted in adown-regulation of the AR, enzalutamide and bicalutamide failed todown-regulate the AR in LNCaP cells (FIG. 41A right panel). Theseeffects occurred without an effect on AR mRNA expression (FIG. 41Abottom panel). Similar to the LNCaP cells, MR49F cells treated with 1002exhibited a significant reduction in AR levels at around 1000 nM that iscomparable to that observed in LNCaP cells (FIG. 41B).

To demonstrate the selectivity of 1002 to AR, the compound was tested invarious cross-reactivity experiments. While 1002 and enzalutamide failedto inhibit the transactivation of GR and mineralocorticoid receptor (MR)(Table 5), it inhibited PR activity by a 4-5 fold weaker potencycompared to the AR antagonistic activity.

To determine the degradation cross-reactivity of 1002, we used variousbreast cancer cell lines that express AR and other receptors. T47D cellsthat express ER and PR, but not AR (although some reports suggest thatT47D cells express AR [39, 40], our clone does not express AR), was usedto evaluate the cross-reactivity of 1002. T47D cells were maintained andtreated similar to that described in FIGS. 41A and 41B and Western blotfor ER, PR, and actin was performed. 1002 failed to down-regulate the ERand PR protein levels (FIG. 41C).

To evaluate the cross-reactivity in a system that expresses all threereceptors (AR, PR, and ER), we used ZR-75-1 breast cancer cells. ZR-75-1cells express all three receptors and the receptors are functional [41].Treatment of ZR-75-1 cells with 1002 resulted in down-regulation of ARprotein levels, but not ER or PR levels (FIG. 41D). This confirms thatunder similar condition 1002 is selective to AR and does not degradeother receptors. These results were reproduced in MDA-MB-453 breastcancer cells that express AR and GR [42, 43], which again shows thedown-regulation of AR, but not GR, by 1002 (data not shown).

Constant protein synthesis will make it difficult to visualize proteindown-regulation. To determine if the observed decrease in AR levels inresponse to 1002 is a result of accelerated degradation, LNCaP cellsmaintained in full-serum-containing medium were treated in a time-coursewith 1002, protein synthesis inhibitor, cycloheximide, or a combinationof cycloheximide and 1002. Treatment of LNCaP cells in 10%scrum-containing condition with 1002 did not decrease the AR levels by10 h of treatment initiation. Cycloheximide treatment resulted in amodest reduction in AR protein levels by 8-10 hours (FIG. 41E). However,when LNCaP cells were treated with a combination of 1002 andcycloheximide, a significant decrease in the AR protein levels wasobserved as early as 4-6 hours. The half-life of AR was reduced by 1002from 10 h (cycloheximide alone) to about 6 h (cycloheximide plus 1002).These results show that the loss of protein in response to 1002 is aresult of enhanced degradation.

1002 requires ubiquitin proteasome pathway to degrade the AR. Todetermine if 1002 ubiquitinated the AR, cells were transfected with ARand HA-tagged ubiquitin and treated with 11 or 1002 in the presence of0.1 nM R1881. 11 was used as positive control in these experiments.Ubiquitin was immunoprecipitated using HA antibody and Western blot forAR was performed. Western blot for AR with non-immunoprecipitatedsamples shows that both 11 and 1002 down-regulated the AR (FIG. 41F).When ubiquitin was immunoprecipitated and AR was detected, the AR wasboth mono- and poly-ubiquitinated by 1002 and 11. The results werereproduced in LNCaP cells treated with 11 or 1002 and AR wasimmunoprecipitated and Western blot for ubiquitin was performed (FIG.41G). Proteasome inhibitor MG132 but not the HSP90 17AAG, enriched theubiquitinated AR in cells treated with 1002 or 11.

The requirement of proteasome pathway for 1002 to down-regulate the ARwas determined by treating LNCaP cells with 1002 and cycloheximide aloneor in combination with a dose response of proteasome inhibitorbortezomib. 1002 and cycloheximide combination down-regulated the AR andthis down-regulation was reversed dose-dependently by bortezomibstarting from 5 μM (FIG. 41H). These results suggest that 1002 requiresubiquitin proteasome pathway to degrade the AR.

We mutated the three known ubiquitin sites in AR (K313, K846, and K848)to arginine (R) and performed Western blots with protein extracts fromcells transfected with the wildtype and mutant ARs and treated with1002. 1002 continued to degrade the wildtype and K-R mutant ARscomparably, indicating that the known ubiquitin sites do not have a rolein 1002-dependent ubiquitin proteasome degradation.

1002 binds to AR AF-1 domain. As molecules of this scaffold uniquelybind to two domains (LBD and AF-1) [26], we evaluated 1002 in variousbiophysical assays for its binding to the AF-1 domain. Earlier studieshave used NMR to determine the interaction between small molecules andlarge proteins [26, 44, 45]. ¹H NMR was utilized to evaluate theinteraction of 1002 with AR AF-1. 1002 (250 μM) was dissolved indeuterated DMSO-ch, and was incubated alone or mixed with 5 μM GST-AF-1and the binding of the molecule to the AF-1 was determined by NMR. 1002in combination with AF-1 provided broad, diffused, and shorter ligandpeaks (FIG. 42A) compared to 1002, revealing that 1002, similar to 11[26], has affinity for AF-1. To further confirm the ¹H NMR results. weperformed WaterLOGSY with 1002 alone or in combination with AF-1. 1002in combination with AF-1 provided a negative signal, characteristic ofbinding to the protein (FIG. 42A).

We performed fluorescence polarization studies with 1002 to confirm thebinding observed with NMR. 1002 was incubated with AR-NTD or AR-AF-1 andthe steady state fluorescence spectra was obtained [46]. 1002 hound tothe AR AF-1 and AR NTD (FIG. 43A) as evident from the shift in thefluorescence peak. reproducing the results obtained with NMR. Unlike thedata shown with 11 [26], no clear quenching of the AR polypeptidesfluorescence was observed with 1002. Previously, quenching was used asan evidence of small molecule binding to the AR-NTD or AF-1 regions.1002 showed a dramatic increase in the fluorescence signal in the regionseen for tyrosine emission (307 nm). Normally, tyrosine signal is notobserved due to energy transfer to tryptophan residues due tofolded/partially folded polypeptides. The increase in the tyrosinesignal is similar to that seen when AR-NTD or AR-AF-1 unfolds/denatures.However, there is no corresponding ‘red shift’ (increase in wavelength)in the tryptophan signal (in urea λmax 344 nm to 347 nm). Although it isdifficult to interpret, it might be possible that 1002 may unfold thereceptor polypeptides (resulting in tyrosine emission), but shields thetryptophan residues.

Raman Spectroscopy confirms an interaction between 1002 and AF-1. It iswell-known that establishing the interaction between the small moleculesand the respective protein whether it is intramolecular hydrogen bondingor van der Waals interactions always leads to a change in the electronicstructure of the reactants. This can be followed by Raman spectroscopy.FIG. 42B presents Raman spectra of AF-1, 1002, and their mixture. Ramanspectrum of protein contains well pronounced peak at ˜1650 cm⁻¹ whichcorresponds to in plane stretch of C═O bonds. This peak corresponds toso-called Amide 1 bond due to the formation of secondary structure inprotein. When 1002 was mixed with AF-1, we observed a red shift in theposition of this peak. The obtained significant shift of 10cm⁻¹ suggeststhat 1002 addition leads to a change in electron distribution in AF-1,which is likely due to their interaction. Shift in band associated withthe stretch of C═O bond is usually associated with formation of hydrogenbonds.

To understand the nature and strength of this interaction further weperformed DFTB theoretical calculations of electron density. DFTBcalculations revealed that there are two possible isomeric structures of1002 which was determined by cis or trans configurations of C═O and N—Hgroups in its structure. The snapshot of interaction between 1002 andamino acid glycine is presented in FIG. 42B. Hydrogen bonds are formedbetween C═O on 1002 and —OH group of glycine. The same carbonyl group in1002 structure participates in the formation of hydrogen bonds withother amino acids. Thus, the selective red shift of C═O bond observed inthe Raman experiment can he directly related to the formation ofhydrogen bond. To understand the strength of interactions between 1002and different amino acids, the binding energies for 1002 and individualamino acids were calculated and results are presented in the table inFIG. 42B. Among all amino acids. 1002 strongly interacts with thattyrosine. phenylalanine, and serine.

Radioactive 1002 confirms the binding of 1002 and conformation change ofAR NTD. Although various biophysical methods indirectly indicate theinteraction of 1002 with the NTD of the AR, we sought to determine thedirect binding of 1002 with the NTD. In order to accomplish this. wecustom-synthesized ³H 1002. Since the binding to AF-1 domain in themicromolar doses, we realized that it is difficult to obtain meaningfulresults due to high background radioactivity. This was solved byadopting a procedure published to discover CBP inhibitor. ICG-001 [47]where G-25 columns were used to reduce the background radioactivity dueto unbound tritium. Protein extracts from cells transfected with vectordid not show any binding with either ³H-1002 or ³H-R1881, while proteinextracts from cells transfected with AR-LBD demonstrated binding with³H-R1881, but not ³H-1002. Protein from cells transfected with AR-NTDdemonstrated a binding to ³H-1002. but not ³H-R1881 (FIG. 43B).

In order to confirm the results, HEK-293 cells were transfected withvector or chimeric constructs, AGG, which expresses AR-NTD, GR-DBD andLBD, or GAA that expresses GR-NTD, AR-DBD and LBD. ³H-1002 bound to AGG,but not to GAA, while ³H-R1881 hound to GAA, but not AGG (FIG. 43B).Finally, AGG transfected cell extracts were incubated with ³H-1002 inthe presence or absence of 100-fold excess of cold 1002. ³H-1002 boundrobustly to AGG, which was competed off by excess cold 1002 (FIG. 43B).These results confirm the direct binding of 1002 to the NTD of AR.

Thermal-shift assay confirms the conformational change of AR-NTD in thepresence of 1002. Cellular thermal-shift assay (CETSA) was recentlydeveloped to detect the binding of molecules to targets in cells 1481.The principle for this assay is based on ligand-hound thermalstabilization of proteins, wherein the target-protein's conformationchanges when hound by a ligand and will be less susceptible totemperature-induced denaturation. Although this procedure was developedfor Western blot, DiscoverX kit uses luminescence to detect thedenaturation. providing a dynamic range. This assay measures the bindingof compounds to a cellular target by detecting changes in proteinthermal-stability. Assay applies enzyme fragment complementationtechnology utilizing β-Galactosidase split into two inactive fragments,the enhanced ProLabel (ePL) peptide and the enzyme acceptor (EA) thatassociates to form a fully active β-Galactosidase enzyme.

AR-LBD transfected showed stabilization in the presence of R1881. whileAR-NTD showed stabilization in the presence of 11. This confirms thebinding of 11 to the AR-NTD that was shown previously by variousbiophysical methods [26]. 11 bound to the AR-NTD starting at 10 μM (FIG.43C). 1002 demonstrated binding to the AR-NTD and increased thestability of the protein. However, 1002 exhibited the binding onlystarting from 80 μM, indicating that it interacts with the AR-NTD weakerthan that 11. Enzalutamide, as expected, failed to stabilize the AR-NTD(FIG. 43C).

N-terminus domain (NTD) of the AR is required for 1002-dependentdegradation. As 1002 binds to both LBD and AF-1 and also degrades theAR, we sought to determine the domain that is required for 1002 todegrade the AR. Since 1002 selectively degraded the AR and not the GR,we obtained AR-GR chimeric receptors to evaluate the domain(s) importantfor the degradation. AR, GR, or AR-GR chimeric receptors (FIG. 44A) weretransfected into cells and the cells were treated with 1002 in thepresence of the respective hormones. As shown earlier, 1002 degraded thefull length AR, but not the GR (FIG. 44B). 1002 also degraded thechimeric protein obtained from fusing AR-NTD to GR DBD and LBD (AGG),but failed to degrade the chimeric protein obtained from fusing GR-NTDto AR-DBD and AR-LBD (GAA). These results suggest that 1002 potentiallyrequires NTD to degrade the AR (FIG. 44B).

Since AR is degraded by ubiquitin-proteasome pathway (FIGS. 41F-H). AGGwas tested to sec if it is still ubiquitinated by 1002. COS cellstransfected with HA-tagged ubiquitin and AR or AGG were treated withvehicle or 10 μM 1002 in the presence of the respective hormones.Protein extracts were immunoprecipitated with HA antibody and Westernblotted with the AR antibody. Interestingly, 1002 increased the mono-and poly-ubiquitinated proteins of AGG (FIG. 44B lower blot), indicatingthat the N-terminus of the AR is important for the ubiquitinationprocess in the presence of 1002.

To determine if the degradation of the AR fusion protein AGG alsotranslates into antagonistic effects, AR, GR, GAA, and AGG weretransfected into cells in combination with GRE-LUC and CMV-renilla LUCand the cells were treated with vehicle. 1002 or enzalutamide in thepresence of the respective hormones. Luciferase assay performed 48 hafter treatment indicated that while both 1002 and enzalutamideantagonized the AR and GAA, due to competitive antagonism, but not GR(FIG. 44C), only 1002 antagonized the transactivation of AGG induced bydexamethasone due to potential down-regulation of the AR-NTD. Theseresults are in concordance with the Western blot results.

Tau5 domain qf AF-1 is required for 1002-dependent AR degradation. Weshowed using NMR that the first generation SARD 11 interacted with thetau domains of the AR AF-1 [26]. To confirm that this domain isimportant for 1002 to degrade the AR, a construct that has the tau5domain deleted was used. Cells were transfected with AR or tau-5-deletedAR, treated with vehicle or 1002 for 48 hours, and a Western blot wasperformed for AR and GAPDH. 1002 degraded the full length AR, but notthe AR construct that has the tau5 domain deleted (FIG. 44D). Inagreement with the degradation data, tau5 domain-deleted AR failed toexhibit an increased ubiquitination over vehicle-treated samples in thepresence of 1002 (FIG. 44D right blot). These results confirm that theSARDs belonging to this scaffold require tau5 domain to interact,ubiquitinate, and degrade the AR.

R isomer and racemate have equal potency as S-isomer of 1002. In orderto ensure that 1002 has a minimal interaction with the LBD that is notcontributing to its functions, we synthesized (R)-isomer (1020) andracemic mixture and evaluated in an AR transactivation assay. The(R)-isomer does not bind to the AR-LBD and hence any observed effect islikely through a different domain. All these molecules antagonized theAR with comparable IC₅₀ (FIG. 44E), confirming the data observed withvarious chimeric and mutant constructs.

1002 does not inhibit the AR function by competitive antagonism. Similarto our earlier publication [26] we evaluated the early expression ofpre-mRNAs in LNCaP cells treated with 1002 in the presence or absence ofR1881 [49]. If 1002 mediates its antagonistic effects throughcompetitive antagonism, then these pre-mRNAs induced by R1881 as earlyas 30 minutes should be inhibited. On the other hand, if degradation isrequired for 1002 to inhibit AR function, then early induction of thepre-mRNAs should not he inhibited as degradation will not be observed asearly as 30 minutes to 2 hours. Treatment of LNCaP cells with 0.1 nMR1881 increased both NDRG I and MT2A pre-mRNAs by 1 hour and theincrease was sustained at 2 and 24 hours (FIG. 44F). 1002 failed toinhibit the expression of the pre-mRNA at 1 and 2 hours, but inhibitedthe expression at 24 hours. These results indicate that 1002 is a truedegrader that requires degradation to elicit its effect and competitivebinding to the LBD, if any, may not have functional significance.

1002 degrades AR-V7 and alter its function: As the SARDs bind to theAF-1 domain and have shown earlier to degrade the AR-SVs [26], we tested1002 in LNCaP cells that stably express inducible AR-V7 [29, 30]. Asdemonstrated earlier, 11 degraded the AR and AR-V7 in this system. 1002down-regulated the AR and AR-V7. indicating that 1002 is an effectivedegrader of both AR and AR-V7 (FIG. 45A left panel). The results werereproduced in LNCaP-95 cells that express AR and AR-V7 (FIG. 45A rightpanel). These effects were observed without any effect on AR-V7 mRNA inLNCaP-ARV7 cells (FIG. 45A bottom panel).

As 1002 degraded the expression of AR-V7, we evaluated the functionalconsequences of this degradation. LNCaP-ARV7 cells were serum starvedfor 48 h and were treated as indicated in FIG. 45B for 24 h in thepresence of 0.1 nM R1881 (left panel) or 10 ng/mL doxycycline (rightpanel). Cells were harvested and the expression of AR-target gene FKBP5and an AR-V7-specific gene EDN2 [29, 30] was measured. Doxycyclineinduced the expression of EDN2, which was inhibited by 1002, but not byenzalutamide, while both enzalutamide and 1002 inhibited the expressionof R1881-induced FKBP5 gene expression (FIG. 45B).

To evaluate whether the effect on the expression of various genes is aresults of an alteration in the occupancy of AR and AR-V7 on the ciselements of target genes, we performed ChIP assay using AR or AR-V7antibodies (FIG. 45C). R1881 induced the recruitment of AR to theregulatory regions of PSA and FKBP5. This recruitment was inhibited by1002 and enzalutamide. AR-V7 recruitment to PSA and EDN2 regulatoryregions was detected upon the addition of doxycycline (due to increasedsynthesis). This recruitment in response to doxycycline was completelyinhibited by 1002, but not by enzalutamide (FIG. 45C).

Genome-wide recruitment analysis of AR and AR-V7 in 22RV1 cellsidentified two AR-V7-selective cis elements that are occupied by AR-V7,but not by AR [50]. We performed ChIP assay with AR-V7 antibody and PCRfor the regulatory regions of these genes was performed. As expected1002. but not enzalutamide, inhibited the recruitment of AR-V7 to FZD6and ZNF32 regulatory regions (FIG. 45D). These results are inconcordance with the results observed with AR-V7 in LNCaP-ARV7 cells.

1002 interacts with a different set of cofactor peptides compared toenzalutamide. To determine if the differences in the properties observedwith 1002 are a result of a distinct interaction with cofactors, wetreated serum-starved LNCaP cells with 10 μM 1002, 11, or enzalutamideor vehicle in the presence of 1 nM DHT. The cells were pretreated withthe drugs or vehicle for 2 hours, followed by a 30 minutes treatmentwith DHT. Protein extracts were subjected to MARCoNI assay where theinteraction of the AR with 154 unique cofactor peptides from 66cofactors was evaluated [51]. 1002 and 11 significantly modulated theAR-cofactor interaction. Although, largely the interaction between ARand cofactors in the presence of 11 and 1002 was similar toenzalutamide, several differences were also observed. Differences in theinteraction of AR with cofactors such as NCoR1 (corepressors) and TREFI(coactivator) observed in SARD-treated samples were not observed incells treated with enzalutamide. These results provide information thatthe AR conformation in the presence of the SARDs is distinct from theconformation in the presence of a competitive antagonist such asenzalutamide.

1002 antagonizes enzalutamide-resistant AR and inhibits theproliferation of enzalutamide-resistant LNCaP cells (MR49F cells). As1002 robustly antagonized and degraded both wildtype andenzalutamide-resistant AR in transient transactivation and Western blotassays, respectively, we evaluated the effect of 1002 on the function ofARs expressed in LNCaP or MR49F cells. LNCaP cells were maintained incharcoal-stripped FBS for 48 h and treated with a dose response of 1002or enzalutamide. RNA was isolated and expression of AR target genes andgrowth was evaluated. Both the compounds inhibited the expression of PSA(top panel) and FKBP5 (middle panel) and growth of LNCaP cells (bottompanel) starting from 100 nM with maximum effect observed at 10 μM (FIG.46A).

The experiment was repeated in MR49F cells that express F876L mutant AR.1002, but not enzalutamide, inhibited the expression of FKBP5 geneinduced by R1881 (FIG. 46B top panel). Concomitant to the geneexpression studies, 1002 inhibited the proliferation of MR49F cells(FIG. 46B bottom panel), while enzalutamide, as expected, failed toinhibit the proliferation of the cells. These anti-proliferative effectsof 1002 is selective to AR-positive prostate cancer cells as 1002 didnot have any effect on the proliferation of AR-negative PC-3 cells (FIG.47A).

1002 inhibits the R1881-induced global gene expression in MR49R cells.As 1002 was effective in inhibiting the expression of FKBP5 in MR49Fcells, we performed a microarray experiment to determine the effect of1002 on R1881-induced global gene expression (FIG. 46C top). Heatmapclearly represents the changes that took place in cells treated withR1881, which robustly altered the expression of approximately 700 genes.Most, if not all, of the genes regulated by R1881 were reversed by 1002to the level observed in vehicle-treated cells. The top genes that wereinhibited by 1002 are all known AR-target genes such as FKBP5, SNAI2,NDRG1, and others. The results indicate that 1002 is effective inreversing the R1881 effect in LNCaP cells expressingenzalutamide-resistant AR. Principal Component Analysis (PCA) plot showsthat the 1002-treated samples cluster with vehicle-treated samples,while R1881-treated samples clustered distinctly. When the genes thatwere not regulated by R1881 were plotted in a separate heatmap, theresults show that 1002 has no effect on these genes (FIG. 46C bottom),indicating that 1002 effects are highly selective to AR pathway and thatit docs not have any off-target effects.

Ingenuity Pathway Analysis (IPA) results indicate that the top fourcanonical pathways that were enriched by the differentially regulatedgenes were cholesterol-synthesizing pathways. While all genes in thepathway were up-regulated by R1881 treatment. 1002 efficiently broughtthe genes down to the vehicle-treated control levels. IPA also indicatethat the genes representing genitourinary oncology pathways aredifferentially regulated, validating the model that was used to generatethe gene expression data.

Drug metabolism and pharmacokinetic (DMPK) studies suggest that 1002 isstable. The half-life of 11 and 17 in liver microsomes was low in therange of 1-20 min [26]. Hence, the first generation SARDs had to beadministered subcutaneously to obtain efficacy in preclinical models.Since CRPC is a chronic disease and patients have to be treated for aprolonged period, orally bioavailable molecules are preferred forclinical development. We used mouse liver microsome (MLM; primarypharmacodynamics (PD) species) to determine the half-life and clearance.1002 had a longer half-life and lower clearance than 11 (Table 6). Thissuggests that 1002 is an appropriate molecule for further development.We also tested the metabolism of 1002 in rat liver microsome (RLM) andin human liver microsome (HLM). 1002 is highly stable in RLM and in HLMby at least 2-4 fold longer than in MLM.

TABLE 6 Comparison across species of stability to co-incubation withliver microsomes DMPK (MLM) DMPK (RLM) DMPK (HLM) T ½ Clearance T ½Clearance T ½ Clearance (mm) μl/min/mg (min) μl/min/mg (min) μl/min/mg1002 77.96 8.9 181 5 274 3 Metabolism properties of SARDs: Livermicrosomes from mouse (MLM), rat (RLM), and human (HLM) were incubatedwith 1002 as indicated in the methods and the amount of compound presentat different points was identified using LC-MS/MS method. Data from bothphase I and II metabolism are presented here. The data are representedas half-life (T_(1/2)) and intrinsic clearance (CL_(int)).

To validate the in vitro data in vivo, 1002 was administered to variousstrains of mice and rats to determine the bioavailability at 6 and 24hours after administration (Table 7). 1002 was highly bioavailable inmice and rats at 6 hours. However, the serum concentration precipitouslydecreased at 24 hours in mice to almost undetectable levels, whilehigher levels in μM range was still observed in rats at 24 hours.

TABLE 7 Bioavailability of 1002 across different strains of mice (NSG,C57BL/6, nude) and rats (S.D. which means Sprague-Dawley) 6 hours 24hours Avg (nM) S.E. (nM) Avg (nM) S.E. (nM) NSG 36025 1138 31 9 C57BL/630386 8850 15 1.4 Nude 41754 6900 38 6 S.D. Rats 5675 339 1725 329Pharmacokinetic properties of 1002. A. 1002 is stable in rats. but notin mice. 1002 (60 mg/kg) dissolved in 15% DMSO + 85% PEG-300 wasadministered orally to the indicated strains and species (n = 3/group).Blood was collected 6 and 24 h after dosing and the amount of 1002remaining in the serum was estimated using LC-MS/MS method.

To validate the results observed at 6 and 24 h a rat PK study wasconducted. Rats were administered with 100-1000 mg/kg of 1002 and theserum concentration was measured over a period of 24 hours. 1002 wasextremely stable in rats with half-life for the 100 and 300 mg/kg doseswas undeterminable due to absence of 50% reduction by 24 hours and theserum concentrations were in the range of 10-50 μM (FIG. 48A). Theseresults are in concordance with the results observed in liver microsomesand suggest that the oral bioavailability of 1002 in CRPC patients maybe appropriate for once daily dosing. Lower doses PK of 1002 in ratsalso provided similar results demonstrating that 1002 is extremelystable (FIG. 48B).

Pharmacodynamic and xenograft studies suggest that 1002 is efficacious:To determine the efficacy of 1002 in vivo a Hershberger assay wasperformed in mice and rats (FIG. 48C). Mice (top panel) wereadministered with 20 or 40 mg/kg 1002 or 30 mg/kg enzalutamide orallyfor 14 days. At the end of 14 days, the animals were sacrificed and theweight of seminal vesicles was recorded. Enzalutamide was not dosedhigher than 30 mg/kg due to its poor solubility. 1002 at 20 and 40 mg/kgreduced the seminal vesicles weight by 10-20 and 50-60%, whileenzalutamide reduced the seminal vesicles weight by 50% (FIG. 48C).

Sprague Dawley rats were dosed with 40 and 60 mg/kg of 1002 orally andenzalutamide at 30 mg/kg for 14 days and the weight of prostate wasrecorded. 1002 reduced the prostate weight by close 90%, whileenzalutamide reduced the prostate weight by 50-60%. This clearly showsthat 1002 is extremely potent in shrinking the prostate potentially dueto its potent antagonistic and degradation effects (FIG. 48C middlepanel). 1002 even after 4 days of dosing reduced the prostate weight byclose to 50%, indicating its ability to antagonize the AR quickly invivo and produce a pharmacodynamics (PD) effect (FIG. 48C bottom panel).

To evaluate the effect of 1002 in an enzalutamide-resistant xenograftmodel. MR49F cells were implanted subcutaneously in NSG mice and oncethe tumors attained 100-200 mm³, the animals were castrated and thetumors were allowed to regrow as CRPC. The animals were treated with 30or 60 mg/kg 1002 and the tumor volume was measured thrice weekly (FIG.49A). 1002 dose-dependently decreased the growth of theenzalutamide-resistant CRPC tumors with 60 mg/kg producing about 75%tumor growth inhibition. Tumor weights recorded at the end of the studyalso indicated that 1002 reduced the tumor weights by approximately60-70% (FIG. 49A bottom panel). Although the PK properties in mice weresub-optimal compared to rats, 1002 produced a marked effect onenzalutamide-resistant tumor growth.

1002 regresses enzalutamide-sensitive and resistant VCaP tumors in NSGrats. Since 1002 is stable in rats compared to mice, we switched over toperforming the xenograft studies in immunocompromised rats (HeraBiolabs, Ky.). We chose two models, one enzalutamide-sensitive parentalVCaP cells and another is enzalutamide-resistant VCaP cells (MDVR).Cells were implanted in SRG rats and once the tumors attained over1000-2000 mm³ volume, the animals were castrated and the tumors wereallowed to regrow as castration-resistant prostate cancer. Once thetumors regrow and attain greater than 2000 mm³, the animals wererandomized and treated orally with vehicle, 30 mg/kg enzalutamide, or 60mg/kg 1002. Tumor volume measurements indicated that while enzalutamideinhibited the growth of parental VCaP xenograft by over 85%, 1002regressed the tumors to unmeasurable levels (FIG. 49B).

As expected, enzalutamide failed to inhibit the enzalutamide-resistantVCaP (MDVR) xenograft. 1002 performance in this tumor model wascomparable to that observed in the parental VCaP xenograft with 1002regressing the tumors to undetectable levels (FIG. 49C). 1002 was alsotested in vitro in the MDVR model and the results show that 1002inhibits the expression of the AR-target genes and its proliferation(FIG. 47B).

Since 1002 regressed the tumors to undetectable levels, we hypothesizedthat this is possible only if the AR is degraded. Western blot in theMDVR tumors demonstrated a significant degradation of the AR in1002-treated samples compared to vehicle-treated samples (FIG. 49C,bottom).

It has not been previously demonstrated that competitive AR antagonistscannot inhibit tumors grown in intact mice or rats. Since 1002 is thefirst orally-bioavailable degrader. we were interested to test theefficacy in intact models, where the animals were not castrated and thetumors grow in the presence of circulating androgens. MDVR tumors grewrobustly in SRG rats and the tumor-hearing animals were treated when thetumors attained over 1500 mm³. One tumor in each group even attained10,000 mm³ when treatment was initiated. While the vehicle- andenzalutamide-treated tumors grew robustly. 1002-treated tumors regressedby over 50% in less than 10-15 days after treatment initiation (FIG.49D, multiple panels for individual animals). We measured serum PSA todetermine i f the tumor volume data is supported by biochemical data.1002 completely inhibited the rising serum PSA to undetectable levelsquickly after treatment initiation (FIG. 49D, 8^(th) panel titled ‘SerumPSA’).

We subsequently conducted a dose response of 1002 in intact SRG ratsbearing MDVR tumors. 1002 at 10 mg/kg inhibited the tumors growth bygreater than 50% and completely inhibited the tumors at 20 and 30 mg/kgdoses (FIG. 49E, top and middle panels). Tumor weights measured at theend of the study and serum PSA (bottom panel) both clearly exhibited adose-dependent inhibition by 1002 (FIG. 49E). Measurement of drugconcentration in the serum and tumor that were collected 24-30 h afterthe last sacrifice demonstrated the accumulation of 1002 in both serumand tumor to the level of over 1-3 μM concentrations (FIG. 48D). Thesteady-state drug concentration even 24 h after the last dose is wellabove the IC₅₀ values of 1002 to inhibit the AR. Immunohistochemistrywith vehicle- and 30 mg/kg 1002 treated specimens clearly indicated that1002 increased the apoptosis as measured by TUNEL staining and inhibitedthe proliferation as measured by Ki67 staining (FIG. 48E). All thesefavorably point to the excellent anti-tumor activity of 1002 inenzalutamide-sensitive and resistant prostate cancers even in intactconditions.

We also tested 1002 in castrated mice to ensure that it does not haveany agonistic activity at higher doses or concentration. Vehicle or 1002(100 mg/kg) was administered orally for 30 days to mice that werecastrated. At the end of 30 days, seminal vesicles were isolated andweighed. Seminal vesicles weight normalized to body weight is expressedas percent change from vehicle control (FIG. 48F). 1002 at such highdoses did not exhibit any agonistic activity as the seminal vesiclesweights were comparable to that of the vehicle-treated animals (FIG. 48Ftop panel). Serum 1002 concentration at the end of 30 days of dosingshowed nice accumulation of 1002 in serum in the range of 1-20 μM (FIG.48F right panel). These results confirm that 1002 is a pure antagonistand does not have any agonistic properties in vivo at higherconcentrations.

In order to determine if the AR is degraded by 1002 in intactconditions, we measured the AR expression by Western blot in proteinextracts from tumors (FIG. 49D at bottom). 1002 robustly degraded theenzalutamide-resistant AR in intact condition (FIG. 49D), demonstratingthat the degradation property translates in vivo. We also evaluatedwhether 1002 degraded the AR at lower doses. Unfortunately, 1002 failedto degrade the AR at 30 mg/kg (data not shown). This potentiallysuggests that higher serum and tumor concentrations are required todegrade the AR and that a tumor regression can he achieved only when theAR is degraded

1002 toxicity profile was acceptable: Since 1002 possessed the requiredproperties for a CRPC drug. we evaluated the toxicity profile of themolecule. 1002 was administered at 100, 300, and 600 mg/kg doses for 7days in Sprague Dawley rats and survival and gross pathology weremonitored. 1002 did not cause any death at 100 mg/kg dose, while deathswere encountered at 300 and 600 mg/kg doses. Gross pathology andhistopathology findings suggest that the deaths in higher dose groupswere due to gastric irritation and inflammation, which could hepotentially avoided using enteric coated capsules or salt forms of 1002.No other pathological observations were detected at any dose. Sinceseveral of the second generation AR antagonists exhibit seizurepotentials, 1002 was also evaluated for its seizure potential in mice.Mice treated with 1002 did not have any seizure, while the positivecontrols exhibited seizures (data not shown). In addition, 1002 alsodoes not have any significant cross-reactivity with GPCRs, kinases, orother nuclear receptors (DiscoverX Eurofin screening) and docs notinhibit hERG channel (Covance). These results suggest that 1002 mighthave a large safety margin and might have no off-target effects.

Discussion. The results provide evidence for an orally bioavailable SARDthat has the necessary drug-like properties for further clinicalevaluation. 1002 degraded the AR and AR-V7 and antagonizedenzalutamide-sensitive and resistant AR and inhibited the growth ofenzalutamide-resistant xenografts. 1002 also possesses appropriate PKproperties showing longer half-life and shorter clearance in rats andhuman liver microsomes than in mouse liver microsomes. This suggeststhat clinically 1002 might require only once daily dosing to observeefficacy.

1002 is effective in two models of enzalutamide-resistance. one with anAR-LBD mutation and another with AR-V7 expression. These two are thecommon forms of resistance observed clinically. Although 30% ofenzalutamide-resistant cancers do not respond at all, the remainingcancers develop resistance shortly after treatment initiation. Mutationsconstitute only a small fraction of the resistance, while AR-SVdevelopment, intra-tumoral androgen synthesis. AR over-expression,coactivators, and altered intracellular signaling pathways allcontribute to resistance development. Degrading the AR and AR-SVs willblock any AR activation by these contributing factors providing asignificant advantage over existing therapeutics. Recently, twomolecules, galeterone and EPI-505, failed in the clinic. After theapproval of enzalutamide and abiraterone in 2012, no other drugstargeting the AR with distinct mechanism of action (apalutamide wasapproved recently, but it is structurally and functionally similar toenzalutamide) have been made available and the patients have notreatment options with distinct mechanisms available to treat the newevolving forms of CRPC. Hence, these SARDs might provide a substantialadvantage to the patients who relapse from enzalutamide.

1002 degrades the AR through ubiquitin proteasome pathway. As ARdegraders have not been successfully identified, characterizing 1002thoroughly is important to demonstrate that it is robust. Most of theproteins are degraded by ubiquitin proteasome pathway and hence weevaluated this pathway first. 1002 treatment resulted in mono- andpoly-ubiquitinated AR. Also, inhibition of proteasome pathway withBortezomib resulted in the reversal of AR degradation suggesting thatthe degradation takes place through proteasome pathway. Only recentlychimeric molecules such as PROTACs and SNIPERS have evolved that havedemonstrated AR degradation characteristics.

However, these molecules are larger than the desired 500 Da size thatare not appropriate for development. With right formulation and dosingthis deficiency can be overcome. As 1002 degrades the AR-SVs and sincethe well-characterized ubiquitin sites in the AR did not play a role inAR degradation by 1002 (FIG. 41I). 1002 might function through newubiquitin sites in the AR-NTD that need to he identified.

This is the first time that an AR-targeting molecule has been shown toexhibit efficacy in xenograft models grown in intact rodents. Sincecirculating testosterone levels are high enough to be competed bycompetitive antagonists, only non-competitive antagonists or degraderswill have the potential to overcome tumors growth in intact animals. Theresults that we observed with enzalutamide-resistant MDVR xenografts isan in vivo confirmation that 1002 is a non-competitive antagonist.Moreover, the dose response and higher dose xenograft studies alsosuggest that tumor shrinkage can only he obtained when the AR isdegraded and not when the AR is just antagonized. These results are thefirst evidence of efficacy of orally bioavailable AR degraders.

Still how AR interacts with its cofactors in the presence of a degraderor a molecule that hinds to a distinct domain or a molecule that doesnot function as a competitive antagonist has not been elucidated. Thisis the first study that provides a glimpse of how such interaction takesplace. We conducted the study in LNCaP prostate cancer cells as opposedto purified system followed by others 1521. Both 1002 and 11, althoughpromoted the interaction of several cofactors with the AR similar tothat of a competitive antagonist enzalutamide. several distinctinteractions were observed in the presence of the two degraders. Theseinteractions will be followed in the future in purified system andcompared to the database of AR interaction with cofactors in thepresence of several other agonists and antagonists.

One of the interesting results observed in this work is that although itis believed that the AR and AR-SVs exist as heterodimers, enzalutamidehad no effect on the recruitment of AR-V7. If they are localized asheterodimer, then enzalutamide should inhibit the recruitment of AR-V7through its effect on AR in both LNCaP-V7 and 22RV1 cells. However,enzalutamide did not affect the recruitment of AR-V7 in either of thesystem, while 1002 successfully inhibited the recruitment, suggestingthat the AR and AR-V7 could be existing as homodimer in these cells andthat the effect cannot be obtained with an LSD-binding AR antagonist andthe drug has to bind to a domain that is common in AR and AR-V7 to blockthe recruitment.

Although the first-generation AR degraders, 11, 17, and others 126, 271,were more potent than 1002 in vitro they were not orally bioavailableand their metabolism properties were not appropriate for drugdevelopment. We had to compromise on the degradation and antagonistproperties to improve the metabolism properties, which has resulted inan excellent molecule that withstood all tests of efficacy and safety.One of the major concerns in AR-targeted drug development is the seizurepotential. 1002 did not exhibit any seizure effects in rodents.

1002 represents a new generation of orally bioavailable molecule thatpossesses necessary characteristics of AR degraders that could bedeveloped clinically. We expect 1002 to overcome enzalutamide resistancein the clinic without having to worry about some of the common safetyproblems.

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Example 19 Competitive, Radioactivity Displacement Assay for NTDBinding: Synthesis of Radioactive SARDs Including ³H-1002 and its Use inan Assay of Competitive Binding to the NTD

We observed that 1002 was a potent androgen receptor (AR) antagonistwith unique properties; however, quizzically we could not demonstratepotent binding to the AR LBD. The canon (recognized rules or scientificlaws) in AR biology is that ligands bind to the ligand binding domain(LBD), but 1002 does not appreciably bind LBD, the canonical bindingsite. Earlier SARDs like 11 and 17 bound competitively to the LBD, i.e.,you can displace 11 or 17 by adding a known LBD hinder. Competitivebinding is the gold standard for demonstrating binding to a particularbinding site and rank ordering ligands by relative binding affinity.

We have struggled to demonstrate that 1002 binds to another(non-canonical) site on the AR. The observed degradation of AR-V7suggested binding to either the N-terminal domain (NTD) or DNA-bindingdomain (DBD). However. no high affinity ligands exist for thesenon-canonical binding sites, so it was impossible to demonstratecompetitive binding to these sites. Instead, we used many biochemicalconstructs [NTD only, LBD only. full-length wildtype AR (NTD-DBD-LBD).full-length chimeric proteins that are part glucocorticoid receptor (GR)and part AR], tested in many biophysical experiments [biolayerinterferometry (BLI), sur face plasmon resonance (SPR), NMR,fluorescence polarization, Raman, cellular thermal shift assay (CETSA)].Consistently we have found that the co-incubation of 1002 (and manyother of our SARDs including 11) with NTD produces data suggestive ofNTD binding. These biophysical techniques are not the gold standard butrather demonstration of competitive binding is industry standard.however no other high affinity NTD binders exist. In light of this, weendeavored to make our own competitive binding assay using radioactive1002 (³H-1002) and attempted to localize radioactivity to the NTDprotein but not LBD, and then displace the radioactivity with cold(non-radioactive) 1002. Radioactive ³H-1002 was purchased from a vendor(Perkin Elmer) but many technical problems delayed the demonstration ofcompetitive binding to NTD (as outlined in Example 18). The technicalproblems were solved and, as demonstrated in Example 18 (FIG. 43B),competitive binding to the NTD has been shown.

Noncompetitive antagonism (or AFI antagonism or NTD antagonism) with anorally active small molecule is novel and unique, and suggestive of ourability to broadly overcome resistance to known agents (all direct(antiandrogens) or indirect (CYP17 inhibitors) LBD binders).Correspondingly, current leads have demonstrated potent in vivo activityin enzalutamide-resistant tumors and many other types of CRPC. Sincemost CRPC tumors grow due to re-activated AR signaling despiteandrogen-deprivation and AR antagonism. only truly androgen-independentprostate cancers (like PC3) theoretically would he beyond the reach ofsuch inhibitors.

Data Examples presented herein are convincing with regard to the abilityof our SARDs to bind the NTD, act as potent and full AR antagonists invivo and produce unprecedented phenotypic changes in vivo. E.g.,chemical castration with a small molecule (1002) and overcoming AR-V7mediated and other types of enzalutamide resistance are unexpected inview of the prior art.

The ability to formulate a competitive NTD binding assay, asdemonstrated in Example 18, allows the skilled artisan to perform assaysto rank order putative NTD-dependent SARD libraries by the appropriatetarget binding affinity (i.e., NTD binding affinity) instead of usingsurrogate markers such as SARD activity or in vivo antagonism asscreening techniques.

Currently there is no publicly available competitive binding assay forNTD binding compounds and no other candidate radioactive NTD bindingligands to formulate such an assay. The discovery of our unique NTDdependent SARDs and their use in this novel competitive NTD-bindingassay may be seminal events in the development of future futuregenerations of prostate cancer therapeutics including treatment of CSPCor CRPC patients that are resistant to all currently known therapies. Inview of the unprecedent assay abilities (i.e., able to screen for NTDbinding) and technical difficulties in formulating the assay, andfurther in view of the unprecedentedly broad spectrum of in vivo ARantagonist and prostate cancer therapeutic activities of the compoundsdiscoverable by the assay, the NTD binding assay of this invention isnovel and unexpected in view of the prior art.

Synthesis of Radioactive SARDs Including ³H-1002

(R)-3-Bromo-N-(4-cyano-2-iodo-5-ttrifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(C₁₂H₉BrF₃IN₂O₂) (1051)

3-Bromo-2-methyl-2-hydroxypropanoic acid (4) (0.50 g, 0.00273224 mol)was reacted with thionyl chloride (0.39 g, 0.0032787 mol),trimethylamine (0.36 g, 0.0035519 mol), and4-amino-5-iodo-2-(trifluoromethyl)benzonitrile (0.81 g, 0.0025956 mol)to afford the titled compound. The product was purified by a silica gelcolumn using DCM and ethyl acetate (9:1) as eluent to afford 0.80 g(64.6%) of the titled compound as a light brown solid.

¹H NMR (400 MHz, CDCl₃) δ 9.53 (s, 1H, NH), 8.92 (s, 1H, ArH), 8.24 (s,1H, ArH), 7.26 (s, 1H, OH), 4.04 (d, J=10.4 Hz, 1H, CH), 3.62 (d, J=10.4Hz, 1H, CH), 1.67 (s, 3H, CH₃).

Mass (ESI, Positive): 479.25[M+H]⁺.

(S)-N-(4-Cyano-2-iodo-5-(trifluoromethyl)phcnyl)-3-(4-fluoro-1H-pyrazol-1-yl)-2-hydroxy-2-methylpropanamide(C₁₅H₁₁F₄IN₄O₂) (1052)

To a solution of 4-fluoro-1H-pyrazole (0.09 g, 0.001048 mol) inanhydrous THF (.5 mL), which was cooled in an ice water bath under anargon atmosphere, was added sodium hydride (60% dispersion in oil, 0.15g, 0.003669 mol). After addition, the resulting mixture was stirred forthree hours.(R)-3-Bromo-N-(4-cyano-2-iodo-5-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(0.50 g, 0.001048 mol) was added to above solution, and the resultingreaction mixture was allowed to stir overnight at room temperature underargon. The reaction was quenched by water and extracted with ethylacetate. The organic layer was washed with brine, dried with MgSO₄,filtered, and concentrated under vacuum. The product was purified by asilica gel column using hexanes and ethyl acetate (2:1 to 1:1) as eluentto afford 0.32 g (64%) of the titled compound as a white solid.

¹H NMR (400 MHz, CDCl₃) δ 9.60 (s, 1H, NH), 8.76 (s, 1H, ArH), 8.69 (s,1H, ArH), 7.76 (d, J=4.8 Hz, 1H, Pyrazole-H), 7.36 (d, J=4.4 Hz, 1H,Pyrazole-H), 6.85 (s, 1H, OH), 4.39 (d, J=14.0 Hz, 1H, CH), 4.20 (d,J=14.0 Hz, 1H, CH), 1.41 (s, 3H, CH₃).

Mass (ESI, Negative): 481.00 [M−H]⁻;

1052 was provided to Perkin Elmer who performed the replacement of theiodine of 1052 with tritium using the reagents shown. In short, 1052 wasreacting the Lindlar palladium in the presence of tritiated hydrogen.

³H-1002 was synthesized as above, analyzed by Perkin Elmer todemonstrate purity and incorporation of radioactivity into ³H-1002. asdescribed below, and formulated into the radioactive competitivedisplacement NTD binding affinity assay described in Example 18.

HPLC analysis of ³H-1002 is shown in FIG. 50 below using the mobilephase, flow rate, and run time indicated in the figure. The HPLCdemonstrates a single peak at around 9.18 minutes indicating the absenceof impurities (FIG. 50A). Further, radioactivity was demonstrated tomigrate with the reaction product, indicating incorporation of thetritium into 1002 to produce ³H-1002 (FIG. 50B). The identity of ³H-1002was further validated by mass spectrometry as demonstrated in FIG. 50Cas a peak m/z 359.43 and possessing 16.24 Ci/mmol of radioactivity (FIG.50D).

General synthesis of radioactive SARDs. Using the reaction intermediate1051 and the chemistry methods described throughout the Examples, avariety of tritiated SARDs can be synthesized and incorporated intovarious NTD binding affinity assays such as described in Example 18.

Novel NTD Binding Affinity Assay:

These experiments used the following protein constructs (peer reviewedliterature providing full descriptions is cited in Example 18):

-   1) AR-LBD is a protein construct only consisting of the LBD domain    of AR (industry standard is to use this construct in AR binding    affinity assays);-   2) AR-NTD is a protein construct only consisting of the NTD domain    of AR;-   3) GAA is a full-length protein in which the NTD is from the GR and    DBD & LBD are from AR; or-   4) AGG is a full-length protein in which the NTD is from the AR and    DBD/LBD are GR.

The top panel of FIG. 43B shows that R1881 binds LBD and 1002 binds NTD:the first two bars act as a negative control, as cells lacking AR-NTDand AR-LBD, i.e. Vector, do not bind R1881 (industrial standard LBDbinding agent) or ³H-1002 (radioactive 1002). The middle pair of barsact as a positive control and demonstrates that R1881 binds to AR-LBDusing this methodology. The right pair of bars demonstrates that ³H-1002hinds to AR-NTD, i.e., 3 to 4-fold higher radioactivity than Vector.Cumulatively, these data confirm our ability to localize radioactivityto the expected binding site, whether LBD or NTD.

The 2^(nd) panel down of FIG. 43B shows that R1881 binds to AR-LBD (GAA)whereas ³H-1002 binds to AR-NTD (AGG). Again, Vector serves as anegative-control and GAA construct serves as positive control (R188I isexpected to binding AR-LBD). ³H-1002 bound to the construct with theAR-NTD (AGG) but not GR-NTD (GAA). i.e., about 2-fold increasedradioactivity.

A column is used to separate the unbound small molecules from the boundsmall molecules, and the enrichment in radioactivity, i.e., ³H-1002binding, is seen in the 3^(rd) panel down of FIG. 43B.

The 3^(rd) panel down (lowest panel) of FIG. 43B demonstrates ourability to displace ³H-1002 from the NTD. Vector is a negative controlin which no AGG (AR is NTD) is present so ³H-1002 should not bind.Middle column shows that ³H-1002 binds AGG (AR is NTD). Right bardemonstrates that adding non-radioactive 1002 at higher concentrationsis able to competitively displace the radioactive ³H-1002.

This data is the first demonstration of competitive binding to the NTD.It conforms to industry standards for demonstrating competitive binding,is easily understood by any biologist that screens for ligand binding,provides compelling data that 1002 and other SARDs of this invention areNTD specific AR antagonists and represents the first orally activenon-competitive AR antagonist. These data help to rationalize theunprecedented activities of 1002 and other pyrazoles such as 1065(compound not reported here; anti-tumor activities in models ofenzalutamide resistance are shown under separate cover) and 1058(anti-tumor activities in models of enzalutamide resistance are shownunder separate cover).

While certain features of the invention have been illustrated anddescribed herein, many modifications, substitutions, changes, andequivalents will now occur to those of ordinary skill in the art. It is,therefore, to be understood that the appended claims are intended tocover all such modifications and changes as fall within the true spiritof the invention

What is claimed is:
 1. A method of treating an androgen receptordependent disease or condition in a subject in need thereof, comprisingadministering to the subject a therapeutically effective amount of aselective androgen receptor degrader (SARD) compound represented by thestructure of formula I

wherein T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR; R¹ is H, CH₃,CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; or T and R¹ form a 3-8 carbocyclicor heterocyclic ring; Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃; Z is H,NO₂, CN, halide, COOH, COR, NHCOR, CONHR, or Y and Z form a 5 to 8membered fused ring; X is CH or N; R is H, alkyl, alkenyl, haloalkyl,alcohol, CH₂CH₂OH, CF₃, CH₂Cl, CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; A isR² or R³: R² is a five or six-membered saturated or unsaturated ringhaving at least one nitrogen atom and 0, 1, or 2 double bonds,optionally substituted with at least one of Q¹, Q², Q³ and Q⁴, eachindependently selected from hydrogen, keto, substituted or unsubstitutedlinear or branched alkyl, substituted or unsubstituted cycloalkyl,substituted or unsubstituted heterocycloalkyl, haloalkyl, CF₃,substituted or unsubstituted aryl, substituted or unsubstituted phenyl,F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR, benzyl, NCS, maleimide,NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR; R³ is NHR², halide, N₃, OR⁴,CF₃, COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴, OCONHR⁴, NHCOOR⁴, NHCONHR⁴,OCOOR⁴, CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴, SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂,SO₂NH(R⁴), SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂, CO(N-heterocycle), NO₂,cyanate, isocyanate, thiocyanate, isothiocyanate, mesylate, tosylate,triflate, PO(OH)₂ or OPO(OH)₂; and R⁴ is H, alkyl, haloalkyl,cycloalkyl, aryl or heteroaryl, wherein said alkyl, haloalkyl,cycloalkyl, aryl or heteroaryl groups are optionally substituted; or itsoptical isomer or a racemic mixture thereof, pharmaceutically acceptablesalt, pharmaceutical product, hydrate or any combination thereof.
 2. Themethod of claim 1, wherein said SARD compound is represented by thestructure of formula IA:

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,hydrate or any combination thereof.
 3. The method of claim 1, whereinsaid SARD compound is represented by the structure of formula IB:

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,hydrate or any combination thereof.
 4. The method of claim 1, whereinsaid SARD compound is represented by the structure of formula II:

wherein T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR; R¹ is H, CH₃,CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; or T and R¹ form a 3-8 carbocyclicor heterocyclic ring; Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃; Z is H,NO₂, CN, halide, COOH, COR, NHCOR, CONHR, or Y and Z form a 5 to 8membered fused ring; X is CH or N; R is H, alkyl, alkenyl, haloalkyl,alcohol, CH₂CH₂OH, CF₃, CH₂Cl, CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; A isR² or R³ R² is a pyrrole, pyrrolidine, pyrazole, pyrazolidine, triazole,imidazole, imidazolidine, or morpholine ring, said ring optionallysubstituted with at least one of Q¹, Q², Q³ and Q⁴, each independentlyselected from hydrogen, keto, substituted or unsubstituted linear orbranched alkyl, substituted or unsubstituted cycloalkyl, substituted orunsubstituted heterocycloalkyl, haloalkyl, CF₃, substituted orunsubstituted aryl, substituted or unsubstituted phenyl, F, Cl, Br, I,CN, hydroxyl, alkoxy, OR, benzyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR,CONHR, COOR or COR; R³ is NHR², halide, N₃, OR⁴, CF₃, COR⁴, COCl,COOCOR⁴, COOR⁴, OCOR⁴, OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴, CN, CONH₂,CONH(R⁴), CON(R⁴)₂, SR⁴. SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴), SO₂N(R⁴)₂,NH₂, NH(R⁴), N(R⁴)₂, CO(N-heterocycle), cyanate, isocyanate,thiocyanate, isothiocyanate, mesylate, tosylate, triflate, PO(OH)₂ orOPO(OH)₂; and R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl,wherein said alkyl, haloalkyl, cycloalkyl, aryl or heteroaryl groups areoptionally substituted; or its optical isomer or a racemic mixturethereof, isomer, pharmaceutically acceptable salt. pharmaceuticalproduct, hydrate or any combination thereof.
 5. The method of claim 4.wherein said SARD compound is represented by the structure of formulaIIA:

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,hydrate or any combination thereof.
 6. The method of claim 4, whereinsaid SARD compound is represented by the structure of formula IIB:

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,hydrate or any combination thereof.
 7. The method of claim 1, whereinsaid SARD compound is represented by the structure of formula VII:

wherein X is CH or N; Y is H, CF₃, F, I, Br, Cl, CN, or C(R)₃; Z is H,NO₂, CN, halide, COON, COR, NHCOR, CONHR, or Y and Z form a 5 to 8membered fused ring; R¹ is H, CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; Tis H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR; or T and R¹ form a 3-8carbocyclic or heterocyclic ring; R is H, alkyl, alkenyl, haloalkyl,alcohol, CH₂CH₂OH, CF₃, CH₂Cl, CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; andQ², Q³ and Q⁴ arc each independently selected from hydrogen, keto,substituted or unsubstituted linear or branched alkyl, substituted orunsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl,haloalkyl, CF₃, substituted or unsubstituted aryl, substituted orunsubstituted phenyl, F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR,arylalkyl, NCS, maleimide, NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR; orits optical isomer or a racemic mixture thereof, pharmaceuticallyacceptable salt, pharmaceutical product, hydrate or any combinationthereof.
 8. The method of claim 7, wherein said SARD compound isrepresented by the structure of formula VIIA:

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,hydrate or any combination thereof.
 9. The method of claim
 7. whereinsaid SARD compound is represented by the structure of formula VIIB:

or its isomer, pharmaceutically acceptable salt, pharmaceutical product,hydrate or any combination thereof.
 10. The method of claim 1, whereinQ¹, Q², Q³ and Q⁴ is hydrogen. CN, NO₂, CF₃, F, Cl, Br, I, NHCOOR,N(R)₂, NHCOR, COR, alkyl, alkoxy, or substituted or unsubstitutedphenyl.
 11. The method of claim I, wherein said SARD compound isrepresented by the structure of any one of the following compounds:


12. The method of claim 1, wherein said androgen receptor dependentdisease or condition in said subject responds to at least one ofAR-splice variant (AR-SV) degradation activity, full length (AR-FL)degradation activity, AR-SV inhibitory, or AR-FL inhibitory activity,comprising administering to the subject a therapeutically effectiveamount of a compound according to claim 1 or claim
 11. 13. The method ofclaim 1, wherein said androgen receptor dependent disease or conditionis breast cancer in said subject.
 14. The method of claim 13, whereinsaid subject has AR expressing breast cancer, AR-SV expressing breastcancer, and/or AR-V7 expressing breast cancer.
 15. The method of claim1, wherein said androgen receptor dependent disease or condition isKennedy's disease in said subject.
 16. The method of claim 1, whereinsaid androgen receptor dependent disease or condition is acne in saidsubject.
 17. The method of claim 16, wherein said acne is acne vulgaris.18. The method of claim 1, wherein said androgen receptor dependentdisease or condition is overproduction of sebum in said subject.
 19. Themethod of claim 18, wherein reducing said overproduction of sebum treatsat least one of seborrhea, seborrheic dermatitis, or acne.
 20. Themethod of claim 1, wherein said androgen receptor dependent disease orcondition is hirsutism or alopecia in said subject.
 21. The method ofclaim 20, wherein said alopecia is at least one of seborrhea, seborrheicdermatitis, or acne at least one of androgenic alopecia, alopeciaareata, alopecia secondary to chemotherapy, alopecia secondary toradiation therapy, alopecia induced by scarring, or alopecia induced bystress.
 22. The method of claim 1, wherein said androgen receptordependent disease or condition is a hormonal disease or condition in afemale in said subject.
 23. The method of claim 22, wherein saidhormonal disease or condition in a female is at least one of precociouspuberty, dysmenorrhea, amenorrhea. multilocular uterus syndrome,endometriosis, hysteromyoma, abnormal uterine bleeding, early menarche,fibrocystic breast disease, fibroids of the uterus, ovarian cysts,polycystic ovary syndrome, pre-eclampsia, eclampsia of pregnancy,preterm labor, premenstrual syndrome, or vaginal dryness.
 24. The methodof claim 1, wherein said androgen receptor dependent disease orcondition is hormonal disease or condition in a male in said subject.25. The method of claim 24, wherein said hormonal disease or conditionin a male is at least one of hypergonadism, hypersexuality, sexualdysfunction, gynecomastia, precocious puberty in a male, alterations incognition and mood, depression, hair loss, hyperandrogenicdermatological disorders, pre-cancerous lesions of the prostate, benignprostate hyperplasia, prostate cancer and/or other androgen-dependentcancers.
 26. The method of claim 1, wherein said androgen receptordependent disease or condition is sexual perversion, hypersexuality, orparaphilias in said subject.
 27. The method of claim 1, wherein saidandrogen receptor dependent disease or condition is androgen psychosisin said subject.
 28. The method of claim 1, wherein said androgenreceptor dependent disease or condition is virilization in said subject.29. The method of claim 1, wherein said androgen receptor dependentdisease or condition is androgen insensitivity syndrome in said subject.30. The method of claim 1, wherein said androgen receptor dependentdisease or condition is AR-expressing cancer in said subject.
 31. Themethod of claim 30, wherein said AR-expressing cancer is at least one ofbreast cancer, testicular cancer, cancers associated with partialandrogen insensitivity syndromes (PAIS) such as gonadal tumors andseminoma, uterine cancer, ovarian cancer, cancer of the fallopian tubesor peritoneum, salivary gland cancer, bladder cancer, urogenital cancer,brain cancer, skin cancer, lymphoma, mantle cell lymphoma, liver cancer,hepatocellular carcinoma, renal cancer, renal cell carcinoma,osteosarcoma, pancreatic cancer, endometrial cancer, lung cancer,non-small cell lung cancer (NSCLC), gastric cancer, colon cancer, perianal adenoma, or central nervous system cancer.
 32. The method of claim1, wherein said androgen receptor dependent disease or condition isamyotrophic lateral sclerosis (ALS) in said subject.
 33. The method ofclaim 1 or claim 11, wherein said androgen receptor dependent disease orcondition is uterine fibroids in said subject.
 34. The method of claim1, wherein said androgen receptor dependent disease or condition isabdominal aortic aneurysm (AAA) in said subject.
 35. A method of claimI, wherein said androgen receptor dependent disease or condition iscaused by polyglutamine (polyQ) AR polymorphs in a subject.
 36. Themethod according to claim 35, wherein the polyQ-AR is a short polyQpolymorph or a long polyQ polymorph.
 37. The method according to claim36, wherein the polyQ-AR is a short polyQ polymorph and the methodfurther treats dermal disease.
 38. The method according to claim 37,wherein the dermal disease is at least one of alopecia, seborrhea.seborrheic dermatitis, or acne.
 39. The method according to claim 36,wherein the polyQ-AR is a long polyQ poly morph and the method furthertreats Kennedy's disease.
 40. A radioactively labeled SARD compoundrepresented by the structure of formula I:

wherein T is H, OH, OR, OCOR, CH₃, —NHCOCH₃, or NHCOR; R¹ is H, CH₃,CH₂F, CHF₂, CF₃, CH₂CH1, or CF₂CF₃; or T and R¹ form a 3-8 carbocyclicor heterocyclic ring; Y is H, CF), F, I, Br, Cl, CN, or C(R)₃; Z is H,NO₂, CN, halide, COOH, COR, NHCOR, CONHR, or Y and Z form a 5 to 8membered fused ring; X is CH or N; R is H, alkyl, alkenyl, haloalkyl,alcohol, CH₂CH₂OH, CF₃, CH₂Cl, CH₂CH₂Cl, aryl, F, Cl, Br, I, or OH; A isR² or R³; R² is a five or six-membered saturated or unsaturated ringhaving at least one nitrogen atom and 0, 1, or 2 double bonds,optionally substituted with at least one of Q¹, Q², Q³ and Q⁴, eachindependently selected from hydrogen, keto, substituted or unsubstitutailinear or branched alkyl, substituted or unsubstituted cycloalkyl,substituted or unsubstituted heterocycloalkyl, haloalkyl, CF₃,substituted or unsubstituted aryl, substituted or unsubstituted phenyl,F, Cl, Br, I, CN, NO₂, hydroxyl, alkoxy, OR, benzyl, NCS, maleimide,NHCOOR, N(R)₂, NHCOR, CONHR, COOR or COR; R³ is NHR², halide, OR⁴, CF₃,COR⁴, COCl, COOCOR⁴, COOR⁴, OCOR⁴, OCONHR⁴, NHCOOR⁴, NHCONHR⁴, OCOOR⁴,CN, CONH₂, CONH(R⁴), CON(R⁴)₂, SR⁴, SO₂R⁴, SOR⁴ SO₃H, SO₂NH₂, SO₂NH(R⁴),SO₂N(R⁴)₂, NH₂, NH(R⁴), N(R⁴)₂, CO(N-heterocycle), NO₂, cyanate,isocyanate, thiocyanate, isothiocyanate, mesylate, tosylate, triflate,PO(OH)₂ or OPO(OH)₂; and R⁴ is H, alkyl, haloalkyl, cycloalkyl, aryl orheteroaryl, wherein said alkyl, haloalkyl, cycloalkyl, aryl orheteroaryl groups are optionally substituted; or its optical isomer or aracemic mixture thereof, isomer, pharmaceutically acceptable salt,pharmaceutical product hydrate or any combination thereof; wherein atleast one of the protons of formula I is replaced by a tritium atom. 41.The compound of claim
 40. wherein said compound is represented by thestructure of ³H-1002:

wherein T is tritium (³H).
 42. An assay for observing and quantitatingthe competitive NTD binding of a candidate NTD binding compound, whereinsaid assay comprises a compound of formula
 40. 43. The assay of claim42, wherein said compound is represented by the structure of ³H-1002:

wherein T is tritium (³H).